8-phenylisoquinolines and pharmaceutical composition used in treatment for sepsis

ABSTRACT

A compound is provided. The compound includes a formula of:

FIELD OF THE INVENTION

The present invention relates to a series of 8-phenylisoquinoline derivatives, and more particularly to a series of 8-phenylisoquinoline derivatives used in treatment for sepsis

BACKGROUND OF THE INVENTION

Sepsis syndrome is a serious whole-body inflammation disease caused by bacteria-released toxins into blood. This syndrome often causes blood coagulation of the patients, and they finally die of multiple organ dysfunction syndromes. According to several epidemiological studies, rates of hospitalization for severe sepsis range from 50 to 300 cases per 100,000 in USA, and the mortality of severe sepsis in ICU ranges from 18% to 55%. The medical cost per patient was estimated from US$26,450 to US$39,100.

In Taiwan, the rate of severe sepsis incidence is 359 per 100,000, and the mortality of severe sepsis is about 30%. The estimated cost for caring a sepsis patient is 866-6505 USD. So far, the main management of sepsis is symptoms relief and vital signs supports, such as using anti-inflammation drugs, antibiotics, blood-vessel constriction drugs and intravenous drips.

Currently, the only one FDA-proved therapeutic agent for reducing mortality of severe sepsis patients and treating sepsis is Drotrecogin alfa (Xigris®). Xigris® is a recombinant human activated protein C by recombinant genetic technology. The recombinant human activated protein C could inhibit the activity of the Factor Va and Factor VIIIa, inhibit the synthesis of the thrombin and inhibit the synthesis of plasminogen activator inhibitor-1 (PAI-1) to regulate the coagulation reaction and possess the features of anti-thrombus and fibrinolysis. However, according to several clinical researches, the benefit effects of Xigris® on reducing mortality of servere sepsis patients is still controversial, so new therapeutic agents for sepsis is still desired.

Serotonin (also called 5-hydroxytryptamine or 5-HT) is a neurotransmitter which could induce coagulation of platelets, contraction of coronary artery. 5-HT_(2A) receptor, which is one subtype of the 5-HT receptor family and a G-protein coupled receptor.

The present 5-HT_(2A) receptor antagonists include sarpogrelate and ketanserin. The method of treatment sepsis using 5-HT_(2A) receptor antagonists is still under research. In order to overcome the drawbacks in the prior art, a novel series of 8-phenylisoquinolines and pharmaceutical composition used in treatment for sepsis is provided.

SUMMARY OF THE INVENTION

In accordance with an aspect of the present invention, a compound is provided. The compound includes a formula of:

In accordance with another aspect of the present invention, A compound or a pharmaceutically acceptable salt thereof is provided. The compound or a pharmaceutically acceptable salt thereof includes a formula of:

-   -   wherein R₁ is one selected from a group consisting of hydrogen,         C₁₋₁₂ linear chain alkyl group, C₁₋₁₂ branched chain alkyl         group, (CH₂)_(n)(Hete)R₁₀R₁₁R₁₂ and (CH₂)_(n)ArR₁₀R₁₁R₁₂,         wherein the n is an integer from 1 to 6, Hete is a heterocyclic         group, and R₁₀, R₁₁ and R₁₂ are independently selected from a         group consisting of hydrogen, halo group, nitro group, amino         group, cyano group, acetyl group, C₁₋₆ linear chain saturated         alkyl group, C₁₋₆ linear chain saturated alkoxy group and C₁₋₆         linear chain saturated haloalkyl group;     -   R₂ is one of a hydrogen and a C₁₋₆ linear chain saturated alkyl         group;     -   R₃ is one of a hydroxyl group and a C₁₋₆ linear chain saturated         alkoxy group;     -   R₄ is one of a hydroxyl group and a C₁₋₆ linear chain saturated         alkoxy group; and     -   X₁, X₂, X₃, X₄ and X₅ are independently selected from a group         consisting of hydrogen, halo group, nitro group, amino group,         cyano group, acetyl group, C₁₋₆ linear chain saturated alkyl         group, C₁₋₆ branched chain saturated alkyl group, C₁₋₆ linear         chain saturated alkoxy group, C₁₋₆ branched chain saturated         alkoxy group, C₁₋₆ linear chain saturated alkylthio group, C₁₋₆         branched chain saturated alkylthio group, C₁₋₆ linear chain         saturated haloalkyl group and C₁₋₆ branched chain saturated         haloalkyl group.

In accordance with a further aspect of the present invention, a pharmaceutical composition is provided. The pharmaceutical composition is provided includes: a pharmaceutically acceptable carrier; and

-   -   a therapeutically effective amount of a compound having a         formula of:

-   -   wherein R₁ is one selected from a group consisting of hydrogen,         C₁₋₁₂ linear chain alkyl group, C₁₋₁₂ branched chain alkyl         group, (CH₂)_(n)(Hete)R₁₀R₁₁R₁₂ and (CH₂)_(n)ArR₁₀R₁₁R₁₂,         wherein the n is an integer from 1 to 6, Hete is a heterocyclic         group, and R₁₀, R₁₁ and R₁₂ are independently selected from a         group consisting of hydrogen, halo group, nitro group, amino         group, cyano group, acetyl group, C₁₋₆ linear chain saturated         alkyl group, C₁₋₆ linear chain saturated alkoxy group and C₁₋₆         linear chain saturated haloalkyl group;     -   R₂ is one of a hydrogen and a C₁₋₆ linear chain saturated alkyl         group;     -   R₃ is one of a hydroxyl group and a C₁₋₆ linear chain saturated         alkoxy group;     -   R₄ is one of a hydroxyl group and a C₁₋₆ linear chain saturated         alkoxy group; and     -   X₁, X₂, X₃, X₄ and X₅ are independently selected from a group         consisting of hydrogen, halo group, nitro group, amino group,         cyano group, acetyl group, C₁₋₆ linear chain saturated alkyl         group, C₁₋₆ branched chain saturated alkyl group, C₁₋₆ linear         chain saturated alkoxy group, C₁₋₆ branched chain saturated         alkoxy group, C₁₋₆ linear chain saturated alkylthio group, C₁₋₆         branched chain saturated alkylthio group, C₁₋₆ linear chain         saturated haloalkyl group and C₁₋₆ branched chain saturated         haloalkyl group.

The excipient or “pharmaceutically acceptable carrier or excipient” or “bioavailable carrier or excipient” includes solvent, dispersant, coating, antimicrobial agent, antifungal agent to preserve or delay-absorbed agent and any other known compound to prepare formulation. In general, these carrier or excipient themselves do not have activity of treating disease. The derivatives disclosed in the present invention in combination with pharmaceutically acceptable carrier or excipient, preparing formulation do not cause adverse effect, allergy or other inappropriate reaction of animals or humans. Therefore, the derivatives disclosed in the present invention in combination with pharmaceutically acceptable carrier or excipient could be applied to human clinically. The formulation of the present invention compound could achieve therapeutic effect through intravenous injection, oral administration, inhalation or through local administration of nose, rectum, vagina or hypoglottis. The 0.1 mg to 100 mg of an active ingredient per day is administrated for different disease of patients.

The carrier is different with different formulation. The composition for sterile injection could be suspended in sterile intravenous injection diluents or solvents, such as 1,3-butanediol. The acceptable carrier could be mannitol or water. In addition, the oil fixed or synthesized monoglyceride/diglyceride suspension medium are commonly used solvents. Fatty acids, such as oleic acid, olive oil, castor oil, glyceride derivatives, especially the polyoxyethylenated form could be prepared for injection and natural pharmaceutically acceptable oil. These oil solution or suspension include long-chain alcohol diluents, dispersant, carboxymethyl cellulose or similar dispersant. Other surfactants for common use include Tween, Spans, other similar emulsifier, pharmaceutically acceptable solid for pharmaceutical manufacture industry, liquid, or other bioavailable enhancer for formulation development.

The composition for oral administration is adapted to oral acceptable formulation, wherein the types include capsule, lozenge, troche, emulsifier, liquid suspension, dispersant and solvent. The common carrier used for oral administration such as lozenge, for example, could be lactose, corn starch, lubricant, magnesium stearate as basic additives. The diluents used for capsule include lactose, dry corn starch. The preparation for liquid suspension or emulsifier formulation is to suspend or dissolve active ingredients with binding emulsifiers or oil interface of suspending agent. The sweetening agents, flavoring agent or coloring matter.

The aerosol sprayer for oral use or inhalation composition is prepared by known formulation technologies. For example, the composition is dissolved in physiological saline, added with benzyl alcohol, other suitable preservative or absorbefacient to enhance bioavailable properties. The composition of the present invention compound could also be prepared to suppository which is administrated through rectum or vagina.

The injections include hypodermic, peritoneal cavity, vein, muscle, joint cavity, intracranial, synovial fluid, intrathecal injection, aorta injection, thoracic injection, lesion injection or other suitable administration technologies.

The above aspects and advantages of the present invention will become apparent to those ordinarily skilled in the art after reviewing the following detailed descriptions and accompanying drawing.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the synthetic scheme 1 of novel derivatives of 8-phenylisoquinoline;

FIG. 2 shows the synthetic scheme 2 of novel derivatives of 8-phenylisoquinoline;

FIG. 3 shows the synthetic scheme 3 of novel derivatives of 8-phenylisoquinoline;

FIG. 4 shows the synthetic scheme 4 of novel derivatives of 8-phenylisoquinoline;

FIG. 5 shows the synthetic scheme 5 of novel derivatives of 8-phenylisoquinoline;

FIG. 6 shows the synthetic scheme 6 of novel derivatives of 8-phenylisoquinoline;

FIG. 7 shows the protective effects of post-treatment of multiple doses of compound 116 on LPS induced endotoxaemia in the mice model;

FIG. 8 shows the protective effects of post-treatment of multiple doses of compound 167 on LPS induced endotoxaemia in the mice model;

FIGS. 9 a-9 d show that compound 116 did not exert platelet activation, but inhibited 5-HT induced amplification of platelet aggregation; and

FIG. 10 shows that compound 116 inhibits serotonin induced rat de-endothelial thoracic descending aorta contraction.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

The present invention will now be described more specifically with reference to the following embodiments. It is to be noted that the following descriptions of preferred embodiments of this invention are presented herein for the purposes of illustration and description only; it is not intended to be exhaustive or to be limited to the precise form disclosed.

The present invention provides a library of novel derivatives of 8-phenylisoquinoline. The synthesis includes the following 6 schemes.

Scheme 1 (FIG. 1): Protection of the hydroxyl group in vanillin with benzyl bromide yielded aldehyde 1 is shown in Scheme 1. Henry reaction between aldehyde 1 and nitromethane gave nitrostyrene 2. Reduction of compound 2 with lithium aluminum hydride in tetrahydrofuran (THF) afforded amine 3. The reaction of amine 3 with an excess amount of methyl formate provided formamide 4. Cyclization of amide 4 using phosphorus oxychloride (POCl₃) via Bischler-Napieralski reaction obtained 3,4-dihydroisoquinoline 5. Alkylation of compound 5 with iodopropane followed by NaBH₄ reduction produced tetrahydroisoquinoline 6 in high yield. Catalytic hydrogenation over Pd/C removed the protective groups of 6 to afford 1,2,3,4-tetrahydroisoquinolin-7-ol 7 in quantitative yield. Treatment of compound 7 with Pb(OAc)₄ in acetic acid followed by acid-catalyzed aromatic substitution with 1,3-dimethoxybenzene using trifluoroacetic acid (TFA) furnished 8-phenyl-tetrahydroisoquinolin-7-ol 8.

Scheme 2 (FIG. 2): The 1-methyl-substituted 8-phenyl-tetrahydroisoquinolin-7-ol derivatives were synthesized starting from amine 3. Treatment of 3 with an excess amount of methyl acetate yielded acetamide 9, which was then converted to 3,4-dihydroisoquinoline 10 using POCl₃. N-Alkylation of 10 with alkyl halides followed by NaBH₄ reduction obtained tetrahydroisoquinolines 11 and 12. The benzyl protecting groups of 11 and 12 were then removed by catalytic hydrogenation to provide phenols 13 and 14, respectively as shown in Scheme 2. Treatment of 13 and 14 with Pb(OAc)₄ in acetic acid followed by acid-catalyzed aromatic substitution with 1,3-dimethoxybenzene using TFA afforded 1-methyl-8-phenyl-tetrahydroisoquinolin-7-ols 15 and 16, respectively.

Scheme 3 (FIG. 3): The N-phenylethyl-substituted 8-phenyl-tetrahydroisoquinolin-7-ol derivatives were synthesized starting from the commercially available 7-hydroxy-6-methoxy-3,4-dihydroisoquinoline (20) as depicted in Scheme 3. N-alkylation of compound 20 with phenylethyl bromide followed by NaBH₄ reduction provided amine 21. Treatment of phenethylamine 21 with Pb(OAc)₄ followed by aromatic substitution with HBr produced 8-bromo-tetrahydroisoquinoline 22. The desired target compounds 29-45 were then synthesized from 22 with various substituted-arylboranes using Suzuki coupling reaction condition in moderate yields.

Scheme 4 (FIG. 4): The N-substituted 8-(2,4-dimethoxyphenyl)-tetrahydroisoquinolin-7-ols were also prepared starting from the commercially available compound 20 as shown in Scheme 4. Treatment of compound 20 with various halides followed by NaBH₄ reduction yielded N-substituted tetrahydroisoquinolin-7-ols 61-76. Oxidation of compounds 61-76 with Pb(OAc)₄ in acetic acid followed by TFA-catalyzed aromatic substitution with 1,3-dimethoxybenzene afforded the corresponding N-substituted 8-(2,4-dimethoxyphenyl)-6-methoxy-tetrahydroisoquinolin-7-ols 101-125, respectively.

Scheme 5 (FIG. 5): Treatment of compound 20 with various 3-phenylpropyl bromides followed by NaBH₄ reduction provided the corresponding N-3-phenylpropyl-substituted tetrahydroisoquinolin-7-ol derivatives 77 and 78 as depicted in Scheme 5. Bromides 97 and 98 were obtained by treatment of compounds 77 and 78 with Pb(OAc)₄ followed by aromatic substitution with HBr, respectively. Aryl coupling reaction of compounds 97 and 98 under Suzuki reaction condition with various substituted-arylboranes afforded the N-3-phenylpropyl-substituted 6-methoxy-8-phenyl-tetrahydroisoquinolin-7-ols 141 and 142 in moderate yields, respectively.

Scheme 6 (FIG. 6): The N-phenylethyl-substituted 6,7-dimethoxy-8-phenyl-tetrahydroisoquinoline derivatives 157-173 were prepared using N-phenylethyl-substituted 8-bromo-6-methoxy-tetrahydroisoquinolin-7-ols 60-96 as depicted in Scheme 6. O-Methylation of phenols 60-96 with methyl iodide in the presence of NaH gaves 6,7-dimethoxy-tetrahydroisoquinolines 150-154, respectively. Aryl coupling reaction of compounds 150-154 with various substituted-arylboranes under Suzuki reaction condition furnished 6,7-dimethoxy-8-phenyl-tetrahydroisoquinolines 157-173, respectively.

The specific synthesizing steps of the compounds from the above schemes 1-6 are as follows:

Compound 7: A mixture of compound 5 (500 mg, 1.87 mmol), C₃H₇Br (0.51 mL, 5.63 mmol), and 2-propanol (17 mL) was refluxed for 16 hours. The resulting solution was concentrated and MeOH (25 mL) was added to dissolve the residue. The solution was cooled in an ice-bath and then NaBH₄ (167 mg, 4.41 mmol) was added slowly under N₂. The mixture was stirred for another 10 minutes and then concentrated. The residue was treated with H₂O and CHCl₃ (35 mL), and then the organic layer was washed with brine, dried over MgSO₄, filtered, and evaporated. The crude residue was chromatographed (silica gel, EtOAc/n-hexane=1:2) to afford compound 6 as a pale yellow solid (442 mg, 1.42 mmol, 76%), which was used in the following reaction without further purification. A mixture of compound 6 (431 mg, 1.38 mmol) and 10% Pd/C (160 mg) in EtOAc (8.5 mL) was stirred under H₂ (1 atm) for 2 hours, and the catalyst was removed by filtration with the aid of Celite. The filtrate was concentrated and the crude residue was chromatographed (silica gel, MeOH/CH₂Cl₂=1:100) to obtain compound 7 as a pale solid (266 mg, 1.20 mmol, 87%).

Compound 21: A mixture of compound 20 (100 mg, 0.56 mmol), 2-phenylethyl bromide (311 mg, 1.68 mmol), and 2-propanol (3.5 mL) was refluxed for 15 hours. The resulting solution was concentrated and MeOH (5 mL) was added to dissolve the residue. The solution was cooled in an ice-bath and then NaBH₄ (49 mg, 1.29 mmol) was added slowly under N₂. The mixture was stirred for another 10 minutes and then concentrated. The residue was treated with H₂O (20 mL) and CHCl₃ (20 mL), and then the organic layer was washed with brine, dried over MgSO₄, filtered, and evaporated. The crude residue was chromatographed (silica gel, MeOH/CH₂Cl₂=1/100) to afford compound 21 as a white solid (146 mg, 0.52 mmol, 92%).

Compound 30: To a solution of C₁₈H₂₀BrNO₂ (50 mg, 0.14 mmol) in 2-propanol (2.0 mL) in a 10-mL thick walled Pyrex reaction vessel, 4-methoxyphenylboronic acid (26 mg, 0.19 mmol) was added. After stirring for 30 min, Pd(OAc)₂ (1.3 mg, 0.006 mmol), PPh₃ (4.7 mg, 0.02 mmol), 2 M Na₂CO_(3(aq)) (0.09 mL, 0.17 mmol), and H₂O (0.1 mL) were added. Then the mixture was heated at 140° C. for 10 min in a microwave synthesizer, and H₂O (0.35 mL) was added before cooling to room temperature. The resulting solution was diluted with H₂O (5 mL) and extracted with EtOAc (5 mL). The organic layer was washed with 5% NaHCO_(3(aq)) and brine. The organic solution was treated with Darco G-60 (100 mg) and stirred at room temperature for 30 min, and then dried over MgSO₄, filtered (the sintered glass funnel was charged with Celite to a depth of 1 cm and Florisil was spread evenly on the top of the Celite), and evaporated. The crude residue was chromatographed (silica gel, EtOAc/n-hexane=2/1) to afford an orange oil (40 mg, 0.10 mmol, 73%).

Compounds 29 and 31-40: Table 1 is a parameter table. “Parameter 1” is added into the reaction vessel for microwave-assisted heating and dissolved with “parameter 2” mL 2-propanol. The appearance of solution is “parameter 3” and the reagent “parameter 4” is added thereinto, and stirred for “parameter 5” minutes. The appearance of resulting solution is “parameter 6”. The Pd(OAc)₂ “parameter 7”, PPh₃ “parameter 8”, 2 M Na₂CO₃(aq) “parameter 9” and “parameter 10” mL H₂O are added and heated “parameter 11”. Before the temperature of the solution is decreased, “parameter 12” mL H₂O is added, stirred in the air until reaching room temperature, diluted with “parameter 13” mL EtOAc, and extracted with “parameter 14” mL H₂O. The organic layer is washed with 5% NaHCO₃(aq), washed with brine, added in “parameter 15” mg Darco G-60, stirred for “parameter 16” minutes, added in MgSO₄ for drying, stirred for “parameter 17” minutes, filtered by the sintered glass funnel covered with about 1 cm of Celite and a thin layer of Florisil, concentrated for drying and purified by flash column chromatography (silica gel, “parameter 18”) to obtain “parameter 19”.

TABLE 1 The parameter table for the synthesis of compounds 29 and 31-40 29 31 32 33 34 35 1 2- C₁₈H₂₀BrNO₂ C₁₈H₂₀BrNO₂ phenylboronic 2-(methylthio)phenyl- 4-(methylthio)phenyl- methoxyphenylboronic (100 mg, (150 mg, 0.41 mmol) acid (43 mg, boronic acid (59 mg, boronic acid (125 mg, acid (65 mg, 0.43 mmol) 0.28 mmol) 0.35 mmol) 0.35 mmol) 0.74 mmol) 2 2.0 2.0 2.0 2.0 2.0 3.0 3 transparent — — — transparent transparent colorless light yellow colorless 4 C₁₈H₂₀BrNO₂ 3-methoxyphenyl- 3,4,5-trimethoxy- C₁₈H₂₀BrNO₂ C₁₈H₂₀BrNO₂ C₁₈H₂₀BrNO₂ (100 mg, boronic acid (62 mg, benzeneboronic (100 mg, 0.28 mmol) (100 mg, 0.28 mmol) (150 mg, 0.41 mmol) 0.28 mmol) 0.41 mmol) acid (106 mg, 0.50 mmol) 5 30 30 10 30 30 25 6 turbid dirt turbid beige turbid beige turbid beige turbid orange turbid white yellow white white white yellow 7 2.5 mg, 0.011 mmol 1.2 mg, 0.005 mmol 1.9 mg, 0.008 mmol 1.9 mg, 0.008 mmol 2.2 mg, 0.01 mmol 2.7 mg, 0.01 mmol 8 5.6 mg, 0.021 mmol 3.1 mg, 0.01 mmol 5.2 mg, 0.02 mmol 5.4 mg, 0.02 mmol 7.0 mg, 0.027 mmol 10 mg, 0.04 mmol 9 0.18 mL, 0.18 mL, 0.27 mL, 0.50 mmol 0.18 mL, 0.34 mmol 0.17 mL, 0.34 mmol 0.25 mL, 0.49 mmol 0.34 mmol 0.34 mmol 10 0.2 0.2 0.3 0.2 0.2 0.3 11 120° C. for 20 120° C. for 10 120° C. for 10 120° C. for 10 140° C. for 20 140° C. for 20 minutes minutes minutes minutes minutes minutes 12 0.7 0.7 1.0 0.7 0.7 1.1 13 10 5 10 10 20 20 14 10 0 0 0 10 20 15 100 100 150 117 106 180 16 5 30 5 15 20 10 17 10 30 10 10 10 10 18 EA/n-hexane = EA/n-hexane = EA/n-hexane = EA/n-hexane = EA/n-hexane = EA/n-hexane = 1/1 1/1 1/1 1/3 1/2 1/2 19 orange light yellow light yellow oil light yellow orange oil orange oil yellow oil oil products products (102 mg, oil products products (66 mg, products (148 mg, products (106 mg, (97 mg, 0.23 mmol, 0.23 mmol, (90 mg, 0.25 mmol, 0.16 mmol, 0.37 mmol, 0.27 mmol, 83%) 55%) 89%) 58%) 89%) 97%) 36 37 38 39 40 1 3,4-(methylenedioxy)benzene 2-cyanophenylboronic acid 2-nitrophenylboronic acid 2-chlorophenylboronic acid 2-acetylphenylboronic acid boronic acid (74 mg, 0.50 mmol) (124 mg, 0.74 mmol) (77 mg, 0.49 mmol) (80 mg, 0.49 mmol) (86 mg, 0.52 mmol) 2 3.0 3.0 3.0 3.0 3.0 3 transparent transparent transparent transparent turbid white light orange light yellow light yellow colorless 4 C₁₈H₂₀BrNO₂ C₁₈H₂₀BrNO₂ C₁₈H₂₀BrNO₂ C₁₈H₂₀BrNO₂ C₁₈H₂₀BrNO₂ (150 mg, (151 mg, (152 mg, 0.42 mmol) (150 mg, 0.41 mmol) (149 mg, 0.41 mmol) 0.41 mmol) 0.42 mmol) 5 30 35 30 25 30 6 turbid beige turbid white turbid light turbid beige turbid beige white yellow white yellow 7 3.0 mg, 0.01 mmol 3.0 mg, 0.01 mmol 4 mg, 0.018 mmol 3.0 mg, 0.01 mmol 3.0 mg, 0.012 mmol 8 11 mg, 0.04 mmol 10 mg, 0.037 mmol 16 mg, 0.06 mmol 11 mg, 0.042 mmol 10 mg, 0.037 mmol 9 0.25 mL, 0.25 mL, 0.37 mL, 0.74 mmol 0.25 mL, 0.49 mmol 0.25 mL, 0.50 mmol 0.49 mmol 0.49 mmol 10 0.3 0.3 0.3 0.3 0.3 11 140° C. for 20 140° C. for 20 120° C. for 20 140° C. for 20 140° C. for 20 minutes minutes minutes minutes minutes 12 1.1 1.1 1.1 1.1 1.1 13 20 20 20 20 20 14 20 20 20 20 20 15 197 195 176 160 150 16 10 10 10 10 10 17 10 10 10 10 10 18 EA/n-hexane = EA/n-hexane = EA/n-hexane = EA/n-hexane = EA/n-hexane = 1/3 1/3 1/2 1/2 1/2 19 white solid light yellow light yellow oil light yellow white solid products (134 mg, oil products products (20 mg, oil products products (40 mg, 0.33 mmol, (33 mg, 0.09 mmol, 0.05 mmol, (105 mg, 0.27 mmol, 0.10 mmol, 81%) 20%) 12%) 65%) 24%)

Compound 44: To a solution of C₁₈H₂₀BrNO₂ (100 mg, 0.28 mmol) in 2-propanol (1.5 mL) in a 10-mL thick walled Pyrex reaction vessel, 3,5-dimethoxybenzeneboronic acid (62 mg, 0.34 mmol) was added. After stirring for 30 min, Pd(OAc)₂ (2.2 mg, 0.01 mmol), PPh₃ (8.0 mg, 0.03 mmol), 2 M Na₂CO_(3(aq)) (0.17 mL, 0.34 mmol), and H₂O (0.7 mL) were added. Then the mixture was heated at 140° C. for 10 min in a microwave synthesizer, and H₂O (0.35 mL) was added before cooling to room temperature. The resulting solution was diluted with H₂O (10 mL) and extracted with EtOAc (10 mL). The organic layer was washed with 5% NaHCO_(3(aq)) (10 mL) and brine. The organic solution was treated with Darco G-60 (100 mg) and stirred at room temperature for 30 min, and then dried over MgSO₄, filtered (the sintered glass funnel was charged with Celite to a depth of 1 cm and Florisil was spread evenly on the top of the Celite), and evaporated. The crude residue was chromatographed (silica gel, EtOAc/n-hexane=1/1) to afford a yellow oil (76 mg, 0.18 mmol, 65%).

Compound 45: To a solution of C₁₈H₂₀BrNO₂ (100 mg, 0.28 mmol) in 2-propanol (2.0 mL) in a 10-mL thick walled Pyrex reaction vessel, 2,3-dimethoxyphenylboronic acid (62 mg, 0.34 mmol) was added. After stirring for 30 min, Pd(OAc)₂ (2.0 mg, 0.009 mmol), PPh₃ (3.7 mg, 0.014 mmol), 2 M Na₂CO_(3(aq)) (0.18 mL, 0.36 mmol), and H₂O (0.2 mL) were added. Then the mixture was heated at 120° C. for 10 min in a microwave synthesizer, and H₂O (0.7 mL) was added before cooling to room temperature. The resulting solution was diluted with H₂O (5 mL) and extracted with EtOAc (5 mL). The organic layer was washed with 5% NaHCO_(3(aq)) (5 mL) and brine. The organic solution was treated with Darco G-60 (100 mg) and stirred at room temperature for 30 min, and then dried over MgSO₄, filtered (the sintered glass funnel was charged with Celite to a depth of 1 cm and Florisil was spread evenly on the top of the Celite), and evaporated. The crude residue was chromatographed (silica gel, EtOAc/n-hexane=1/1) to afford a yellow oil (82 mg, 0.20 mmol, 71%).

Compounds 60, 85 and 95-98: Table 2 is a parameter table. The starting material “parameter 1” is added into a reaction flask at room temperature under N₂, and “parameter 2” mL HOAc is added thereinto. The Pb(OAc)₄ “parameter 3” is added, and then the solution is “parameter 4”, poured into the conical flask and added with “parameter 5” mL Na₂CO₃ (sat) slowly. The pH of the aqueous layer is alkaline (pH=“parameter 6”). The solids produced in neutralization is filtered. The filter cake is washed with CH₂Cl₂. The filtrate is extracted with “parameter 7” mL CH₂Cl₂. The organic layer is washed with brine, added with MgSO₄ for drying, stirred for 5 minutes, filtered with the sintered glass funnel and concentrated for drying to obtain “parameter 8” product. The crude product was used in the following reaction without further purification.

The solution which is added in HBr “parameter 9” in the room temperature air and the appearance of the solution is “parameter 10”. After stirring for “parameter 11” hours, “parameter 12” mL Na₂CO₃ (sat) and “parameter 13” mL CH₂Cl₂ are added slowly to the solution. The pH of the aqueous layer is alkaline (pH=“parameter 14”), and then the “parameter 15” mL CH₂Cl₂ and “parameter 16” mL H₂O are added for extraction. The organic layer is washed with brine, added with MgSO₄ for drying, stirred for 5 minutes, filtered with the sintered glass funnel and concentrated for drying to obtain crude product “parameter 17” mg. The “parameter 19” is afforded after flash column chromatography (silica gel, “parameter 18”).

TABLE 2 The parameter table for the synthesis of compounds 60, 85 and 95-98 60 85 95 96 97 98 1 C₁₈H₂₁NO₂ C₁₈H₂₀N₂O₄ C₁₈H₂₀ClNO₂ C₁₈H₂₀FNO₂ C₁₉H₂₂N₂O₄ C₁₉H₂₂N₂O₄ (351 mg, 1.24 mmol) (503 mg, 1.53 mmol) (1000 mg, (1002 mg, (320 mg, 0.93 mmol) (285 mg, 0.83 mmol) 3.15 mmol) 3.32 mmol) 2 6.2 7.6 15.5 16.5 4.7 4.2 mL 3 830 mg, 1.87 mmol 1034 mg, 2.33 mmol 2101 mg, 4.74 mmol 2262 mg, 5.10 mmol 636 mg, 1.43 mmol 562 mg, 1.27 mmol 4 deep red transparent transparent transparent red brown tranparent red coffee color red coffee deep red burgundy red brown color brown 5 40 60 100 130 25 25 6 8-9 8-9 8-9 8-9 8-9 8-9 7 50 80 100 130 40 40 8 deep orange red brown red brown red brown deep orange brown oil red solid (282 mg, solid (498 mg, solid (1089 mg, solid (1088 mg, red solid (303 mg, (263 mg, 0.66 mmol) 0.83 mmol) 1.29 mmol) 2.91 mmol) 3.04 mmol) 0.76 mmol) 9 6 mL, 48% wt 10 mL, 48% 15 mL, 48% 15 mL, 48% 5 mL, 48% wt 5 mL, 48% wt wt wt wt 10 turbid yellow turbid orange turbid orange turbid orange turbid orange turbid orange 11 3 2 1.5 1.5 1 0.5 12 35 70 100 100 35 35 13 20 50 50 50 20 20 14 8-9 8-9 9-10 9-10 8-9 8-9 15 15 50 80 60 20 50 16 0 30 30 10 0 0 17 344 433 1013 973 225 195 18 EA/n-hexane = EA/n-hexane = MeOH/CH₂Cl₂ = EA/n-hexane = MeOH/CH₂Cl₂ = MeOH/CH₂Cl₂ = 1/2 1/1 1/100 1/3 1/100 1/90 19 beige white yellow solid white solid white solid orange yellow orange yellow solid products products (363 mg, products (747 mg, products (752 mg, oil products oil products (260 mg, 0.72 mmol, 0.89 mmol, 1.88 mmol, 1.98 mmol, (179 mg, 0.42 mmol, (170 mg, 0.40 mmol, 58%) 59%) 60%) 60%) 46%) 49%)

Compounds 63-67, 67-70 and 74-78: Table 3 is a parameter table. The starting material “parameter 1” is added into a flask at room temperature under N₂, and then the “parameter 2” mL IPA and “parameter 3” are added thereinto. The starting material is dissolved at “parameter 4” ° C. The appearances of reaction solution are “parameter 5” and “parameter 7” in about “parameter 6” minutes, and then the solution is heated at 110˜120° C. for “parameter 8” hours and concentrated in room temperature. The “parameter 9” mL MeOH is added and the resulting mixture is stirred for “parameter 10” minutes. To the solution which is “parameter 11” in a ice-bath, is added NaBH₄(s) “parameter 12” slowly under N₂ and stirred for “parameter 13” minutes. The solution which is “parameter 14” is added with “parameter 15” mL H₂O and extracted with “parameter 16” mL CHCl₃. The organic layer is added with MgSO₄ for drying, stirred for “parameter 17” minutes, filtered, and concentrated to obtain “parameter 18”. The “parameter 20” is afforded after flash column chromatography (silica gel, “parameter 19”).

TABLE 3 The parameter table for the synthesis of compounds 63-67, 67-70 and 74-78 63 64 65 66 67 69 1 C₁₀H₁₁NO₂ C₁₀H₁₁NO₂ C₁₀H₁₁NO₂ C₁₀H₁₁NO₂ C₁₀H₁₁NO₂ C₁₀H₁₁NO₂ (20, 300 mg, (20, 300 mg, (20, 1001 mg, (20, 301 mg, (20, 300 mg, (20, 300 mg, 1.69 mmol) 1.69 mmol) 5.65 mmol) 1.70 mmol) 1.69 mmol) 1.69 mmol) 2 10 10 35 14 10 10 3 C₈H₈NO₂Br C₈H₈NO₂Br C₈H₈NO₂Br 4-chlorophenethyl C₈H₇BrCl₂ C₈H₈Br₂ (1127 mg, (866 mg, 3.76 mmol) (3810 mg, bromide (1.00 g, 3.94 mmol) (1.00 g, 3.79 mmol) 4.89 mmol) 16.56 mmol) (1115 mg, 5.08 mmol) 4 60 75 — 80 80 80 5 transparent transparent — transparent transparent transparent light yellow light yellow yellow yellow yellow 6 30 10 — 120 120 90 7 turbid turbid yellow transparent turbid yellow turbid yellow turbid yellow yellow orange yellow 8 18 16 17 24 25 19 9 15 15 35 15 15 15 10 10 10 10 10 10 10 11 turbid turbid yellow — transparent transparent transparent yellow yellow yellow yellow 12 264 mg, 206 mg, 3.39 mmol 853 mg, 22.53 mmol 576 mg, 15.2 mmol 257 mg, 6.78 mmol 270 mg, 7.14 mmol 6.97 mmol 13 20 20 10 20 20 20 14 turbid turbid orange — opaque orange opaque opaque yellow orange orange 15 30 0 0 30 30 30 16 30 30 100 30 30 30 17 5 5 5 5 5 5 18 orange solid orange solid — orange solid orange solid orange solid crude crude produts crude produts crude produts crude produts produts 19 MeOH/CH₂Cl₂ = MeOH/CH₂Cl₂ = MeOH/CH₂Cl₂ = MeOH/CH₂Cl₂ = MeOH/CH₂Cl₂ = MeOH/CH₂Cl₂ = 1/60 1/60 1/80 1/90 1/100 1/100 20 canary white solid beige yellow white solid yellow solid white solid yellow solid products (541 mg, solid products products (448 mg, products (442 mg, products products 1.65 mmol, (1558 mg, 1.41 mmol, 1.26 mmol, (626 mg, (439 mg, 97%) 4.74 mmol, 81%) 74%) 1.73 mmol, 1.34 mmol, 84%) 102%) 79%) 70 74 75 76 77 78 1 C₁₀H₁₁NO₂ C₁₀H₁₁NO₂ C₁₀H₁₁NO₂ C₁₀H₁₁NO₂ C₁₀H₁₁NO₂ C₁₀H₁₁NO₂ (20, 301 mg, (20, 300 mg, (20, 1002 mg, (20, 1000 mg, (20, 300 mg, (20, 300 mg, 1.70 mmol) 1.69 mmol) 5.64 mmol) 5.64 mmol) 1.69 mmol) 1.69 mmol) 2 10 10 35 35 10 10 3 C₁₀H₁₃O₂Br C₁₀H₁₃O₂Br 2-chlorophenethyl 2-fluorophenethyl C₉H₁₀BrNO₂ C₉H₁₀BrNO₂ (1.0 g, 4.65 mmol) (1.0 g, 4.08 mmol) bromide bromide (1215 mg, (989 mg, (3716 mg, (3438 mg, 4.98 mmol) 4.05 mmol) 16.93 mmol) 16.93 mmol) 4 70 80 80 80 88 75 5 transparent transparent transparent transparent transparent transparent light yellow orange yellow yellow orange white white 6 120 120 — — 210 60 7 turbid turbid yellow — — turbid yellow turbid yellow yellow 8 19 18 17 18 19.5 19.5 9 15 15 35 35 15 15 10 — — 10 10 10 10 11 transparent transparent turbid yellow transparent turbid yellow turbid yellow yellow orange yellow light brown 12 272 mg, 270 mg, 7.13 mmol 825 mg, 21.8 mmol 836 mg, 22.1 mmol 266 mg, 7.03 mmol 271 mg, 7.16 mmol 7.17 mmol 13 20 20 20 20 20 20 14 transparent transparent opaque pinky opaque pinky transparent transparent orange orange orange orange brown light orange 15 30 30 100 100 30 30 16 30 30 100 100 30 30 17 5 5 5 5 5 5 18 orange solid orange yellow light orange light orange orange oil orange oil products solid products solid products solid products products products 19 MeOH/CH₂Cl₂ = MeOH/CH₂Cl₂ = MeOH/CH₂Cl₂ = MeOH/CH₂Cl₂ = MeOH/CH₂Cl₂ = MeOH/CH₂Cl₂ = 1/100 1/60 1/90 1/90 1/90 1/90 20 white solid beige white white solid white solid yellow oil yellow oil products solid products products (1601 mg, products products (503 mg, products (504 mg, 452 mg, 1.32 mmol, 5.04 mmol, (1501 mg, 1.47 mmol, (492 mg, 1.61 mmol, 78%) 89%) 4.98 mmol, 87%) 1.44 mmol, 95%) 88%) 85%)

Compound 68: A mixture of C₁₀H₁₁NO₂ (300 mg, 1.69 mmol), C₈H₈Br₂ (1.00 g, 3.79 mmol), and 2-propanol (10 mL) was heated to reflux for 23 h. The resulting solution was cooled to room temperature, and evaporated. The crude was dissolved in MeOH (15 mL), cooled to 0° C. in ice-bath, and then NaBH₄ (420 mg, 11.1 mmol) was added in portions under N₂. The mixture was stirred for another 20 min and then concentrated. The residue was treated with CHCl₃ (30 mL) and H₂O (30 mL) and then the organic layer was dried over MgSO₄, filtered and evaporated. The purification is performed by the precipitation method. The crude product is dissolved with 5 mL of EtOAc, and then the product is precipitates with 10 mL of n-hexane to afford a beige solid (620 mg, 1.71 mmol).

Compound 121: To a solution of C₁₉H₂₃NO₂ (250 mg, 0.84 mmol) in HOAc (4.2 mL), Pb(OAc)₄ (579 mg, 1.31 mmol) was added and the mixture was stirred at room temperature under N₂ for 15 min. The reaction mixture was diluted with CH₂Cl₂ and Na₂CO_(3(sat)) (20 mL) was added slowly. The solids formed in neutralization were removed by filtration and washed with CH₂Cl₂. The combined filtrate was extracted with CH₂Cl₂ (35 mL), and then the organic layer was washed with brine, dried over MgSO₄, filtered, and evaporated to afford a brown oil (480 mg, 1.35 mmol), which was used in the following reaction without further purification. To a solution of the crude oil in CH₂Cl₂ (17 mL), 1,3-dimethoxybenzene (0.17 mL, 1.3 mmol) and trifluoroacetic acid (0.84 mL) were added. The resulting mixture was stirred at room temperature for 30 min, and then Na₂CO_(3(sat)) (20 mL) was added slowly. The resulting solution was extracted with CH₂Cl₂ (18 mL) and then the organic layer was washed brine, dried over MgSO₄, filtered, and evaporated. The crude residue was chromatographed (silica gel, MeOH/CH₂Cl₂=1/10) to afford a red-brown oil (214 mg, 0.49 mmol, 59%).

Compounds 105-110, 114-116, 120, 122, 123 and 125: Table 4 is a parameter table. The starting material “parameter 1” is added into the flask at room temperature under N₂ and dissolved with “parameter 2” mL HOAc. The solution which is “parameter 3” is added with Pb(OAc)₄ “parameter 4”, and then the resulting solution which is “parameter 5” is stirred for “parameter 6” minutes, poured into the 125 mL conical flask, stirred and added slowly with “parameter 7” mL Na₂CO_(3(sat)). The pH of the aqueous layer is alkaline (pH=8-9). The solid produced by neutralization is filtered and washed with CH₂Cl₂. The filtrate is extracted with “parameter 8” mL CH₂Cl₂. The organic layer is washed with brine, added with MgSO₄ for drying, stirred for 5 minutes, filtered, and concentrated to afford “parameter 9”. The crude product is used in the following reaction without further purification.

The crude product is dissolved with “parameter 10” mL CH₂Cl₂ at room temperature under N₂. The solution which is “parameter 11” is added with 1,3-dimethoxybenzene “parameter 12” and trifluoroacetic acid “parameter 13”. The color of the solution turns into “parameter 14”. After the solution is stirred for “parameter 15” minutes, “parameter 16” mL Na₂CO_(3(sat)) is added slowly. The pH of the aqueous layer is alkaline (pH=8-9), and “parameter 17” mL CH₂Cl₂ is added for extraction. The organic layer is washed with brine, added with MgSO₄ for drying, stirred for 5 minutes, filtered, and concentrated to obtain “parameter 18” mg crude product. The “parameter 20” is afforded after flash column chromatography (silica gel, “parameter 19”).

TABLE 4 The parameter table for the synthesis of compounds 105-110, 114-116, 120, 122, 123 and 125 105 106 107 108 109 1 C₁₈H₂₀N₂O₄ C₁₈H₂₀ClNO₂ C₁₈H₁₉Cl₂NO₂ (250 mg, C₁₈H₂₀BrNO₂ C₁₈H₂₀BrNO₂ (250 mg, (160 mg, 0.50 mmol 0.71 mmol) (250 mg, 0.69 mmol) (250 mg, 0.69 mmol) 0.76 mmol) 2   3.8   2.5   3.6   3.5   3.6 3 transparent transparent transparent light transparent light transparent light light yellow light yellow green yellow green 4 509 mg, 337 mg, 0.76 mmol 473 mg, 1.07 mmol 459 mg, 1.04 mmol 470 mg, 1.06 mmol 1.15 mmol 5 transparent deep coffee red black transparent transparent red brown color coffee color coffee color 6 15 60 27 15 15 7 25 20 25 40 25 8 40 40 50 35 9 red coffee coffee color oil red coffe color oil deep coffee red coffee color color oil products (218 mg, products (291 mg, color oil oil products products 0.58 mmol) 0.71 mmol) products (214 mg, (262 mg, 0.62 mmol) (240 mg, 0.51 mmol) 0.62 mmol) 10 15 12 14 10 13 11 transparent transparent red transparent red transparent red transparent red deep red coffee color coffee color coffee color coffee color brown 12 0.14 mL, 0.11 mL, 0.87 mmol 0.14 mL, 1.06 mmol 0.10 mL, 0.77 mmol 0.12 mL, 0.93 mmol 1.1 mmol 13 0.73 mL 0.58 mL 0.71 mL 0.51 mL 0.62 mL 14 transparent transparent red transparent red transparent red transparent red deep black coffee brown coffee brown to coffee brown to coffee brown to tea color to to transparent transparent light transparent light transparent light transparent light coffee coffee color coffee color coffee color tea color color 15 30 60 30 30 70 16 25 10 20 30 15 17 20 23 26 30 27 18 480  327  490  325  342  19 EA/n-hexane = MeOH/CH₂Cl₂/ MeOH/CH₂Cl₂/NH₄OH = MeOH/CH₂Cl₂/ EtOAc/n-hexane = 1/1 NH₄OH = 1/100/0.1 NH₄OH = 1/2 1/100/0.1 1/100/0.1 20 light orange coffee color oil coffee color oil red coffee color light brown oil yellow solid products (130 mg, products (152 mg, oil products (39 mg, products (80 mg, products 0.29 mmol, 0.31 mmol, 44%) 0.11 mmol, 0.18 mmol, (151 mg, 57%) 11%) 26%) 0.33 mmol, 43%) 110 114 115 116 120 1 C₁₉H₂₃NO₃ C₁₉H₂₃NO₂ C₁₈H₂₀ClNO₂ (250 mg, C₁₈H₂₀FNO₂ C₁₉H₂₃NO₃ (250 mg, (250 mg, (250 mg, 0.73 mmol) 0.79 mmol) (251 mg, 0.83 mmol) 0.798 mmol) 0.80 mmol) 2  4   3.7  4   4.2  4 3 transparent transparent transparent light light orange light yellow light yellow light yellow orange yellow yellow 4 569 mg, 505 mg, 1.14 mmol 570 mg, 1.29 mmol 605 mg, 1.36 mmol 532 mg, 1.20 mmol 1.28 mmol 5 transparent transparent red translucent red translucent red deep coffee red coffee coffee color coffee color coffee color color color 6 15 15 15 15 15 7 25 30 25 25 25 8 40 35 35 35 35 9 red coffee red coffee red coffee color oil red coffee color red coffee color color oil color oil products (300 mg, oil products oil products products products (253 mg, 0.80 mmol) (285 mg, 0.79 mmol) (290 mg, 0.781 mmol) (243 mg, 0.63 mmol) 0.65 mmol) 10 13 13 16 16 16 11 transparent coffee color transparent red transparent red transparent red red coffee coffee color coffee color coffee color color 12 0.13 mL, 0.13 mL, 0.95 mmol 0.16 mL, 1.2 mmol 0.16 mL, 1.2 mmol 0.15 mL, 1.2 mmol 0.98 mmol 13 0.65 mL 0.63 mL 0.79 mL 0.79 mL 0.78 mL 14 transparent coffee color to transparent red transparent red transparent red red coffee light coffee coffee color to coffee color to coffee color to color to color transparent light transparent light transparent transparent coffee color coffee color coffee color light coffee color 15 30 30 30 30 30 16 20 20 25 20 25 17 22 22 19 19 19 18 450  433  480  417  560  19 EA/n-hexane = MeOH/CH₂Cl₂ = EA/n-hexane = 1/2 MeOH/CH₂Cl₂/ MeOH/CH₂Cl₂/ 1/1 1/100 NH₄OH = NH₄OH = 1/100/0.1 1/100/0.1 20 light brown red coffee orange solid light orange coffee color oil oil products color oil products (128 mg, yellow solid products (162 mg, (217 mg, products (129 mg, 0.28 mmol, 36%) products (126 mg, 0.36 mmol, 0.48 mmol, 0.26 mmol, 0.29 mmol, 45%) 60%) 36%) 35%) 122 123 125 1 C₁₈H₂₀ClNO₂ C₁₉H₂₃NO₃ C₁₉H₂₃NO₂ (251 mg, (250 mg, (250 mg, 0.80 mmol) 0.84 mmol) 0.79 mmol) 2   4.2  4   4.3 3 transparent transparent transparent light orange orange yellow orange yellow yellow 4 540 mg, 578 mg, 1.30 mmol 580 mg, 1.31 mmol 1.22 mmol) 5 deep coffee deep coffee transparent red color color coffee color 6 17 15 15 7 25 25 35 8 35 35 35 9 red coffee deep red coffee red coffee color oil color oil color oil products (283 mg, products products (290 mg, 0.80 mmol) (286 mg, 0.78 mmol) 0.76 mmol) 10 13 16 16 11 transparent transparent transparent red red coffee deep red coffee coffee color color color 12 0.15 mL, 0.15 mL, 1.2 mmol 0.16 mL, 1.2 mmol 1.1 mmol 13 0.76 mL 0.78 m 0.8 mL 14 transparent transparent transparent deep red coffee deep red coffee red coffee color to color to color to deep transparent light transparent coffee color coffee color coffee color 15 33 30 30 16 25 25 25 17 22 19 19 18 430  430  506  19 EA/n-hexane = EA/n-hexane = MeOH/CH₂Cl₂ = 1/1 1/1 1/200 20 orange light brown oil light orange yellow yellow solid products (140 mg, solid products (135 mg, products 0.31 mmol, 0.31 mmol, (151 mg, 39%) 37%) 0.33 mmol, 42%)

Compounds 141 and 142: Table 5 is a parameter table. “Parameter 1” and 2-methoxyphenylboronic acid (46 mg, 0.30 mmol) are added into the reaction vessel for microwave-assisted heating and dissolved with 2-propanol (2 mL), and stirred for 30 minutes. Pd(OAc)₂ “parameter 2”, PPh₃ “parameter 3”, 2 M Na₂CO_(3(aq)) (0.14 mL, 0.28 mmol), and H₂O (0.2 mL) are added and the mixture is heated at 120° C. for 20 minutes using microwave synthesizer. Before the temperature of the solution is decreased, the solution us added H₂O (0.7 mL), stirred in the air until reaching room temperature, diluted with 10 mL of EtOAc, and extracted with 10 mL of H₂O. The organic layer is washed with 5% NaHCO_(3(aq)), washed with brine, added in “parameter 4” mg Darco G-60, stirred for 10 minutes, added in MgSO₄ for drying, stirred for 10 minutes, filtered by the sintered glass funnel covered with about 1 cm of Celite and a thin layer of Florisil, concentrated. The crude product is purified by flash column chromatography (silica gel, “parameter 5”) to obtain a yellow oil “parameter 6”. Free base “parameter 7” is dissolved in CH₂Cl₂, and then a solution of HCl in CH₂Cl₂ is added until pH=1. The resulting mixture is concentrated to obtain hydrochloride salt “parameter 8”.

TABLE 5 The parameter table for the synthesis of compounds 141 and 142 141 142 1 103 mg, 0.24 mmol 104 mg, 0.25 mmol 2 1.4 mg, 0.006 mmol 2.0 mg, 0.009 mmol 3 6.5 mg, 0.024 mmol 5.9 mg, 0.022 mmol 4 112 117 5 1/4 2/1 6 88 mg, 0.20 mmol, 76 mg, 0.17 mmol, 83% 72% 7 83 mg, 0.20 mmol 18 mg, 0.04 mmol 8 beige white solid light yellow oil products (100 mg, products (20 mg, 0.20 mmol) 0.04 mmol)

Compound 150: To a solution of C₁₈H₂₀BrNO₂ (100 mg, 0.28 mmol) in DMF (2 mL), trimethylphenyl-ammonium chloride ((CH₃)₃PhNCl, 102 mg, 0.59 mmol) and t-BuOK (67 mg, 0.60 mmol) were added. The suspension was heated to 60° C. under N₂ for 3.5 h, and then (CH₃)₃PhNCl (102 mg, 0.59 mmol) was added and heated to 70° C. for 4.5 h. After cooling to room temperature, the reaction mixture was treated with CHCl₃ (10 mL) and 5% NaOH_((aq)) (20 mL). The organic layer was washed with brine, dried over MgSO₄, filtered, and evaporated. The crude residue was chromatographed (silica gel, EtOAc/n-hexane=1/4) to afford a yellow solid (83 mg, 0.22 mmol, 79%).

Compound 152: To a solution of C₁₈H₁₉BrN₂O₄ (406 mg, 1.00 mmol) in DMF (9 mL), which was cooled to 0° C. and degassed, NaH (40 mg, 1.67 mmol) and CH₃I (0.06 mL, 0.98 mmol) in DMF (1 mL) were added. After stirring for 10 min, NH₄Cl (111 mg, 2.08 mmol) was added, and then the reaction mixture was treated with diethyl ether (100 mL) and H₂O (100 mL). The organic layer was washed with brine, dried over MgSO₄, filtered and evaporated. The crude residue was chromatographed (silica gel, EtOAc/n-hexane=1/2) to afford a yellow solid (123 mg, 0.29 mmol, 30%).

Compound 153: To a solution of C₁₈H₁₉BrClNO₂ (300 mg, 0.75 mmol) in DMF (6 mL), (CH₃)₃PhNCl (542 mg, 3.16 mmol) and t-BuOK (333 mg, 2.97 mmol) were added. The suspension was heated to 60° C. under N₂ for 16 h, and then heated to 70° C. for 1 h. After cooling to room temperature, the reaction mixture was treated with Et₂O (100 mL) and H₂O (100 mL). The organic layer was washed with brine, dried over MgSO₄, filtered, and evaporated. The crude residue was chromatographed (silica gel, EtOAc/n-hexane=1/4) to afford a white solid (189 mg, 0.46 mmol, 61%).

Compound 154: To a solution of C₁₈H₁₉BrFNO₂ (400 mg, 1.05 mmol) in DMF (8 mL), (CH₃)₃PhNCl (727 mg, 4.23 mmol) and t-BuOK (468 mg, 4.17 mmol) were added. The suspension was heated to 70° C. under N₂ for 16 h. After cooling to room temperature, the reaction mixture was treated with Et₂O (100 mL) and H₂O (100 mL). The organic layer was washed with brine, dried over MgSO₄, filtered, and evaporated. The crude residue was chromatographed (silica gel, EtOAc/n-hexane=1/4) to afford a white solid (247 mg, 0.63 mmol, 60%).

Compounds 157-159, 165-168 and 171-173: Table 6 is a parameter table. “Parameter 1” is added into the reaction vessel for microwave-assisted heating and dissolved with “parameter 2” mL 2-propanol. “Parameter 3” is added thereinto, and stirred for 30 minutes. Pd(OAc)₂ “parameter 4”, PPh₃ “parameter 5”, 2 M Na₂CO_(3(aq)) “parameter 6” and “parameter 7” mL H₂O are added and heated to 120° C. for 20 min using microwave synthesizer. Before the temperature of the solution is decreased, “parameter 8” mL H₂O is added, and then cooled to room temperature, diluted with 10 mL EtOAc, and extracted with 10 mL H₂O. The organic layer is washed with 5% NaHCO_(3(aq)) followed by brine, added in “parameter 9” mg Darco G-60, stirred for 10 min, filtered by the sintered glass funnel covered with about 1 cm of Celite and a thin layer of Florisil, concentrated, and purified by flash column chromatography (silica gel, “parameter 10”) to obtain “parameter 11”.

TABLE 6 The parameter table for the synthesis of compounds 157-159, 165-168 and 171-173 157 158 159 165 166 1 2-fluorophenylboronic 2-chlorophenylboronic 2-methoxyphenylboronic 2-fluorophenylboronic 2-chlorophenylboronic acid (58 mg, acid (55 mg, acid acid (55 mg, acid (60 mg, 0.41 mmol) 0.35 mmol) (55 mg, 0.36 mmol) 0.39 mmol) 0.38 mmol) 2 2 1.8 1.8 2 2 3 C₁₉H₂₄BrNO₂ C₁₉H₂₄BrNO₂ C₁₉H₂₄BrNO₂ C₁₉H₂₁BrFNO2 C₁₉H₂₁BrFNO₂ (102 mg, 0.27 mmol) (90 mg, 0.24 mmol) (89 mg, 0.24 mmol) (105 mg, 0.27 mmol) (101 mg, 0.26 mmol) 4 1.5 mg, 0.007 mmol 1.6 mg, 0.007 mmol 1.7 mg, 0.0076 mmol 1.6 mg, 0.007 mmol 1.4 mg, 0.006 mmol 5 4.2 mg, 0.016 mmol 8.0 mg, 0.03 mmol 4.7 mg, 0.018 mmol 6.0 mg, 0.023 mmol 5.6 mg, 0.021 mmol 6 0.20 mL, 0.40 mmol 0.18 mL, 0.36 mmol 0.18 mL, 0.36 mmol 0.19 mL, 0.38 mmol 0.19 mL, 0.38 mmol 7 0.2 0.18 0.18 0.2 0.2 8 0.7 0.63 0.63 0.7 0.7 9 117 113 99 101 117 10 1/3 1/3 1/2 1/4 1/4 11 beige yellow oil light yellow oil light yellow oil yellow oil light yellow oil products (103 mg, products (58 mg, products (69 mg, products (108 mg, products (50 mg, 0.26 mmol, 0.14 mmol, 0.17 mmol, 0.26 mmol, 0.12 mmol, 97%) 59%) 71%) 99%) 47%) 12 C₂₅H₂₆FNO₂ C₂₅H₂₆ClNO₂ C₂₆H₂₉NO₃ (69 mg, C₂₅H₂₅F₂NO₂ C₂₅H₂₅ClFNO₂ (103 mg, 0.26 mmol) (31 mg, 0.08 mmol) 0.17 mmol) (108 mg, 0.26 mmol) (50 mg, 0.12 mmol) 13 white solid light yellow light yellow light yellow beige white products (113 mg, solid products solid products solid products solid muriate 0.26 mmol) (36 mg, 0.08 mmol) (66 mg, 0.15 mmol) (116 mg, 0.26 mmol) products (55 mg, 0.12 mmol) 167 168 171 172 173 1 2-fluorophenylboronic 2-chlorophenylboronic 2-fluorophenylboronic 2-chlorophenylboronic 2-methoxyphenylboronic acid (45 mg, acid (48 mg, acid (50 mg, acid (56 mg, acid 0.32 mmol) 0.31 mmol) 0.36 mmol) 0.36 mmol) (56 mg, 0.37 mmol) 2 1.8 1.7 2 2 2 3 C₁₉H₂₁BrClNO₂ C₁₉H₂₁BrClNO₂ C₁₉H₂₂BrN₂O₄ C₁₉H₂₂BrN₂O₄ C₁₉H₂₂BrN₂O₄ (90 mg, 0.22 mmol) (84 mg, 0.20 mmol) (98 mg, 0.23 mmol (100 mg, 0.24 mmol) (101 mg, 0.24 mmol) 4 2.0 mg, 0.009 mmol 1.0 mg, 0.004 mmol) 1.7 mg, 0.0076 mmol 1.8 mg, 0.0072 mmol 1.8 mg, 0.008 mmol 5 4.7 mg, 0.02 mmol 4.4 mg, 0.02 mmol 5.7 mg, 0.022 mmol 6.0 mg, 0.023 mmol 6.5 mg, 0.025 mmol 6 0.19 mL, 0.38 mmol 0.16 mL, 0.32 mmol 0.18 mL, 0.36 mmol 0.18 mL, 0.36 mmol 0.18 mL, 0.36 mmol 7 0.2 0.17 0.2 0.2 0.2 8 0.7 0.6 0.7 0.7 0.7 9 105 90 112 101 115 10 1/3 1/3 1/1 1/2 1/1 11 yellow oil beige yellow beige solid beige white beige yellow products (91 mg, solid products products (75 mg, solid products solid products 0.21 mmol, (66 mg, 0.15 mmol, mg, 0.17 mmol, (72 mg, 0.16 mmol, (88 mg, 0.20 mmol, 97%) 73%) 71%) 66%) 81%) 12 C₂₅H₂₅ClFNO₂ C₂₅H₂₅Cl₂NO₂ C₂₅H₂₅FN₂O₄ C₂₅H₂₅ClN₂O₄ C₂₆H₂₈N₂O₅ (72 mg, (91 mg, 0.21 mmol) (66 mg, 0.15 mmol) (56 mg, 0.13 mmol) (72 mg, 0.16 mmol) 0.16 mmol) 13 light yellow beige solid beige white beige yellow beige white solid products products (72 mg, solid products solid products solid products (94 mg, 0.20 mmol) 0.15 mmol) (61 mg, 0.13 mmol) (81 mg, 0.17 mmol) (80 mg, 0.16 mmol)

TABLE 7 The analytical data of the compounds in this invention Compound number 7 Name 6-Methoxy-2-propyl-1,2,3,4-tetrahydroisoquinolin- 7-ol ¹H NMR δ 0.84 (t, J = 7.3 Hz, 3H), 1.47-1.59 (m, 2H), (200 MHz, CDCl₃) 2.33-2.41 (m, 2H), 2.64 (d, J = 4.8 Hz, 2H), 2.71 (d, J = 4.8 Hz, 2H), 3.70 (s, 3H), 3.89 (s, 2H), 6.04 (s, 1H), 6.41 (s, 1H), 6.43 (s, 1H) ¹³C NMR δ 12.5, 20.4, 28.7, 51.5, 55.7, 56.2, 60.8, 111.2, (50 MHz, CDCl₃) 113.2, 125.4, 127.1, 144.5, 146.2 ESI-MS m/z 222 ([M + H]⁺) EIHR-MS calcd for C₁₃H₁₉NO₂ [M]+, 221.1416; found, 221.1442 Compound number 8 Name 8-(2,4-Dimethoxyphenyl)-6-methoxy-2-propyl- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 0.85 (t, J = 7.3 Hz, 3H), 1.38-1.53 (m, 2H), (200 MHz, CDCl₃) 2.26-2.37 (m, 3H), 2.63-2.72 (m, 2H), 2.85-2.91 (m, 2H), 3.17 (s, 2H), 3.72 (s, 3H), 3.85 (s, 3H), 3.86 (s, 3H), 6.55-6.61 (m, 3H), 7.00-7.05 (m, 1H) ¹³C NMR δ 12.4, 20.6, 29.6, 50.9, 54.6, 55.8, 56.0, 56.3, 60.7, (50 MHz, CDCl₃) 99.4, 105.1, 110.5, 116.8, 122.9, 125.5, 127.1, 132.2, 141.7, 145.5, 158.5, 161.0 EIHR-MS calcd for C₂₁H₂₇NO₄ [M]⁺, 357.1940; found, 357.1915. Compound number 10 Name 7-(Benzyloxy)-6-methoxy-1-methyl-3,4- dihydroisoquinoline ¹H NMR δ 2.25 (s, 3H), 2.62 (t, J = 7.6 Hz, 2H), 3.57-3.61 (200 MHz, CDCl₃) (m, 2H), 3.91 (s, 3H), 5.15 (s, 2H), 6.69 (s, 1H), 7.01 (s, 1H), 7.34-7.48 (m, 5H) ¹³C NMR δ 23.8, 26.3, 47.4, 56.5, 72.2, 111.1, 113.0, 122.8, (50 MHz, CDCl₃) 128.0, 128.5, 129.1, 132.3, 137.5, 146.9, 152.2, 164.3. Compound number 11 Name 7-(Benzyloxy)-6-methoxy-1,2-dimethyl-1,2,3,4- tetrahydroisoquinoline ¹H NMR δ 1.32 (d, J = 6.7 Hz, 3H), 2.48 (s, 3H), 2.65-2.74 (200 MHz, CDCl₃) (m, 1H), 2.78-2.84 (m, 2H), 3.00-3.11 (m, 1H), 3.56 (q, J = 6.5 Hz, 1H), 3.84 (s, 3H), 5.10 (s, 2H), 6.59 (s, 1H), 6.60 (s, 1H), 7.23-7.45 (m, 5H) ¹³C NMR δ 20.0, 27.5, 43.0, 49.1, 56.4, 59.1, 71.8, 112.1, (50 MHz, CDCl₃) 113.5, 126.6, 127.8, 128.2, 128.9, 131.1, 137.7, 146.8, 148.7. Compound number 12 Name 7-(Benzyloxy)-6-methoxy-1-methyl-2-propyl- 1,2,3,4-tetrahydroisoquinoline ¹H NMR δ 0.97 (t, J = 7.4 Hz, 3H), 1.68 (d, J = 6.8 Hz, 3H), (200 MHz, CDCl₃) 1.96-2.02 (m, 2H), 2.92-2.99 (m, 2H), 3.01-3.03 (m, 1H), 3.08-3.13 (m, 1H), 3.35-3.41 (m, 1H), 3.46-3.53 (m, 1H), 3.86 (s, 3H), 4.41 (d, J = 6.8 Hz, 1H), 5.08-5.15 (m, 2H), 6.62 (s, 1H), 6.66 (s, 1H), 7.29-7.45 (m, 5H) ¹³C NMR δ 11.2, 18.2, 20.1, 22.9, 43.5, 53.7, 55.9, 57.3, 71.2, (100 MHz, CDCl₃) 111.5, 112.5, 122.4, 124.7, 127.3, 127.8, 128.4, 136.4, 147.3, 149.5 EIHR-MS calcd for C₂₁H₂₇NO₂ [M]+, 325.2042; found, 325.2022. Compound number 13 Name 6-Methoxy-1,2-dimethyl-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 1.59 (d, J = 6.7 Hz, 3H), 2.87 (s, 3H), 3.00-3.07 (200 MHz, CD₃OD) (m, 2H), 3.34-3.38 (m, 1H), 3.49-3.63 (m, 1H), 3.84 (s, 3H), 4.34 (q, J = 6.7 Hz, 1H), 6.63 (s, 1H), 6.75 (s, 1H) ¹³C NMR δ 19.0, 24.5, 39.9, 47.8, 56.4, 60.1, 112.4, 114.2, (50 MHz, CD₃OD) 122.1, 126.5, 147.0, 149.1. Compound number 14 Name 6-Methoxy-1-methyl-2-propyl-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 0.88 (t, J = 7.3 Hz, 3H), 1.66 (d, J = 6.7 Hz, 3H), (400 MHz, CDCl₃) 1.86-1.98 (m, 2H), 2.94-3.03 (m, 2H), 3.04-3.09 (m, 2H), 3.39-3.41 (m, 1H), 3.45-3.50 (m, 1H), 3.76 (s, 3H), 4.41 (q, J = 6.6 Hz, 1H), 6.56 (s, 1H), 6.60 (s, 1H) ¹³C NMR δ 11.1, 17.7, 20.0, 22.5, 43.6, 53.4, 56.0, 57.5, (100 MHz, CDCl₃) 110.7, 112.4, 120.4, 124.2, 145.1, 146.8 EIHR-MS calcd for C₁₄H₂₁NO₂ [M]⁺, 235.1572; found, 235.1601. Compound number 15 Name 8-(2,4-Dimethoxyphenyl)-6-methoxy-1,2-dimethyl- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 1.02 (d, J = 8.0 Hz, 3H), 2.56 (s, 3H), 2.77 (dd, (400 MHz, CDCl₃) J = 16.0, 4.0 Hz, 1H), 2.93-2.98 (m, 1H), 3.06-3.16 (m, 1H), 3.22-3.31 (m, 1H), 3.77 (s, 3H), 3.86 (s, 3H), 3.88 (s, 3H), 6.58-6.61 (m, 2H), 6.63 (s, 1H), 6.98 (dd, J = 6.1, 2.8 Hz, 1H) ¹³C NMR δ 16.1, 25.3, 41.4, 44.1, 55.5, 55.7, 55.9, 99.3, (100 MHz, CDCl₃) 105.1, 110.4, 116.1, 122.7, 123.2, 128.7, 131.5, 142.3, 145.5, 158.5, 160.0 EIHR-MS calcd for C₂₀H₂₅NO₄ [M]⁺, 343.1784; found, 343.1791. Compound number 16 Name 8-(2,4-Dimethoxyphenyl)-6-methoxy-1-methyl-2- propyl-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 0.87 (t, J = 8.0 Hz, 3H), 0.98 (d, J = 4.0 Hz, 3H), (400 MHz, CDCl₃) 1.49 (q, J = 8.0 Hz, 2H), 2.44-2.54 (m, 3H), 2.85- 2.88 (m, 1H), 2.90-3.05 (m, 1H), 3.19-3.30 (m, 1H), 3.55 (q, J = 8.0 Hz, 1H), 3.72 (s, 3H), 3.86 (s, 3H), 3.87 (s, 3H), 5.30 (s, 1H), 6.57-6.62 (m, 3H), 7.10 (d, J = 8.0 Hz, 1H) ¹³C NMR δ 12.1, 19.3, 21.3, 24.7, 42.8, 53.1, 55.46, 55.49, (100 MHz, CDCl₃) 55.6, 55.9, 99.2, 104.7, 110.6, 116.4, 122.9, 124.3, 132.6, 133.3, 141.4, 145.1, 157.5, 160.8 ESI-MS m/z 371.0 [M]⁺ Compound number 21 Name 6-Methoxy-2-phenethyl-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.71-2.96 (m, 8H), 3.61 (s, 2H), 3.84 (s, 3H), 6.57 (200 MHz, CDCl₃) (s, 2H), 7.16-7.34 (m, 5H) ¹³C NMR δ 28.8, 34.1, 51.2, 55.6, 56.0, 60.4, 110.8, 112.4, (50 MHz, CDCl₃) 125.5, 126.2, 127.3, 128.5, 128.9, 140.5, 143.8, 145.4 Compound number 29 Name 6-Methoxy-8-(2-methoxyphenyl)-2-phenethyl- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.57-2.66 (m, 2H), 2.72-2.81 (m, 4H), 2.85-2.92 (200 MHz, CDCl₃) (m, 2H), 3.25 (s, 2H), 3.74 (s, 3H), 3.86 (s, 3H), 6.63 (s, 1H), 6.97-7.06 (m, 2H), 7.11-7.28 (m, 6H), 7.32-7.40 (m, 1H) ¹³C NMR δ 29.2, 34.0, 50.5, 54.2, 55.7, 56.0, 60.0, 110.2, (50 MHz, CDCl₃) 111.3, 120.9, 122.8, 124.1, 125.2, 126.0, 126.2, 128.4, 128.7, 129.3, 131.6, 140.5, 141.1, 145.2, 157.1 ESI-MS m/z 390 ([M + H]⁺) EIHR-MS calcd for C₂₅H₂₈NO₃ [M + H]⁺, 390.2069; found, 390.2054 Compound number 30 Name 6-Methoxy-8-(4-methoxyphenyl)-2-phenethyl- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.59-2.68 (m, 2H), 2.73-2.82 (m, 4H), 2.92, (t, (200 MHz, CDCl₃) J = 5.8 Hz, 2H), 3.29 (s, 2H), 3.83 (s, 3H), 3.87 (s, 3H), 6.62 (s, 1H), 6.93-6.94, (m, 1H), 6.98-6.99 (m, 1H), 7.12-7.24 (m, 7H) ¹³C NMR δ 29.4, 34.0, 50.6, 55.0, 55.3, 56.1, 60.2, 110.0, (50 MHz, CDCl₃) 114.1, 125.4, 125.9, 126.0, 127.6, 128.4, 128.7, 130.9, 140.4, 141.2, 145.4, 158.9 ESI-MS m/z 390 ([M + H]⁺), 412 ([M + Na]⁺) EIHR-MS calcd for C₂₅H₂₈NO₃ [M + H]⁺, 390.2069; found, 390.2067 Compound number 31 Name 6-Methoxy-8-(3-methoxyphenyl)-2-phenethyl- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.59-2.68 (m, 2H), 2.74-2.80 (m, 4H), 2.89-2.95 (200 MHz, CDCl₃) (m, 2H), 3.31 (s, 2H), 3.78 (s, 3H), 3.86 (s, 3H), 6.63 (s, 1H), 6.78-6.83, (m, 2H), 6.86-6.94 (m, 1H), 7.11-7.24 (m, 5H), 7.30-7.40 (m. 1H) ¹³C NMR δ 29.2, 33.8, 50.4, 54.7, 55.2, 56.0, 60.0, 110.1, (50 MHz, CDCl₃) 113.3, 115.2, 122.1, 125.3, 125.4, 126.1, 126.2, 128.4, 128.7, 129.6, 136.9, 140.3, 141.0, 145.4, 159.7 ESI-MS m/z 390.2 ([M + H]⁺), 412.2 ([M + Na]⁺) EIHR-MS calcd for C₂₅H₂₈NO₃ [M + H]⁺, 390.2069; found, 390.2064 Compound number 32 Name 6-Methoxy-8-(3,4,5-trimethoxyphenyl)-2- phenethyl-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.62-2.71 (m, 2H), 2.78-2.85 (m, 4H), 2.91-2.96 (200 MHz, CDCl₃) (m, 2H), 3.32 (s, 2H), 3.90 (s, 6H), 3.91 (s, 3H), 3.92 (s, 3H), 5.41 (s, 1H), 6.46 (s, 2H), 6.65 (s, 1H), 7.13-7.30 (m, 5H) ¹³C NMR δ 29.5, 34.1, 50.5, 54.5, 56.2, 60.3, 61.0, 106.6, (50 MHz, CDCl₃) 110.3, 125.7, 126.2, 126.3, 128.5, 128.8, 131.0, 137.1, 140.3, 140.9, 145.4, 153.5 ESI-MS m/z 449 ([M]⁺) EIHR-MS calcd for C₂₇H₃₂NO₅ [M + H]⁺, 450.2280; found, 450.2268 Compound number 33 Name 6-Methoxy-2-phenethyl-8-phenyl-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.57-2.66 (m, 2H), 2.72-2.79 (m, 4H), 2.89-2.94 (200 MHz, CDCl₃) (m, 2H, 3.28 (s, 2H), 3.85 (s, 3H), 6.63 (s, 1H), 7.10-7.14 (m, 2H), 7.19-7.25 (m, 5H), 7.32-7.48 (m, 3H) ¹³C NMR δ 29.3, 33.9, 50.5, 54.9, 56.1, 60.1, 110.1, 125.4, (50 MHz, CDCl₃) 126.1, 126.4, 127.5, 128.4, 128.6, 128.7, 129.8, 135.7, 140.3, 141.0, 145.4 ESI-MS m/z 360 ([M + H]⁺) EIHR-MS calcd for C₂₄H₂₆NO₂ [M + H]⁺, 360.1964; found, 360.1956 Compound number 34 Name 6-Methoxy-8-(2-methylthiophenyl)-2-phenethyl- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.37 (s, 3H), 2.57-2.66 (m, 2H), 2.72-2.81 (m, (200 MHz, CDCl₃) 4H), 2.89-2.92 (m, 2H), 3.22 (s, 2H), 3.88 (s, 3H), 6.67 (s, 1H), 7.12-7.22 (m, 8H), 7.25-7.29 (m, 1H) ¹³C NMR δ 15.2, 29.2, 34.0, 50.5, 53.8, 56.0, 60.0, 110.6, (50 MHz, CDCl₃) 124.1, 124.7, 125.0, 125.6, 125.9, 126.1, 128.4, 128.6, 128.8, 130.1, 133.9, 138.6, 140.5, 141.0, 145.2 ESI-MS m/z 406 ([M + H]⁺) EIHR-MS calcd for C₂₅H₂₈NO₂S [M + H]⁺, 406.1841; found, 406.1836 Compound number 35 Name 6-Methoxy-8-(4-methylthiophenyl)-2-phenethyl- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.51 (s, 3H), 2.63-2.68 (m, 2H), 2.74-2.81 (m, (200 MHz, CDCl₃) 4H), 2.89-2.95 (m, 2H), 3.29 (s, 2H), 3.88 (s, 3H), 6.63 (s, 1H), 7.14-7.21 (m, 6H), 7.25-7.33 (m, 3H) ¹³C NMR δ 15.7, 29.4, 33.9, 50.5, 55.0, 56.1, 60.2, 110.1, (50 MHz, CDCl₃) 125.5, 125.6, 126.1, 126.5, 128.4, 128.8, 130.3, 137.6, 140.4, 141.1, 145.4 ESI-MS 406 ([M + H]⁺) EIHR-MS calcd for C₂₅H₂₈NO₂S [M + H]⁺, 406.1841; found, 406.1839 Compound number 36 Name 8-(Benzo[1,3]dioxol-5-yl)-6-methoxy-2-phenethyl- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.61-2.70 (m, 2H), 2.73-2.84 (m, 4H), 2.89-2.94 (200 MHz, CDCl₃) (m, 2H), 3.30 (s, 2H), 3.88 (s, 3H), 5.43 (bs, 1H), 6.00 (bs, 2H), 6.63 (s, 1H), 6.68-6.73 (m, 2H), 6.86- 6.90 (m, 1H), 7.16-7.26 (m, 5H) ¹³C NMR δ 29.5, 34.1, 50.6, 55.0, 56.2, 60.3, 101.2, 108.7, (50 MHz, CDCl₃) 110.1, 110.4, 123.1, 125.5, 125.9, 126.1, 128.5, 128.8, 129.0, 140.4, 141.2, 145.3, 147.0, 147.8 ESI-MS m/z 404 ([M + H]⁺) EIHR-MS calcd for C₂₅H₂₆NO₄ [M + H]⁺, 404.1862; found, 404.1849 Compound number 37 Name 8-(2-Cyanophenyl)-6methoxy-2-phenethyl-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.61-2.80 (m, 6H), 2.87-2.94 (m, 2H), 3.12 (d, J = (200 MHz, CDCl₃) 14.8 Hz, 1H), 3.32 (d, J = 14.9 Hz, 1H), 3.90 (s, 3H), 6.68 (s, 1H), 7.12-7.29 (m, 5H), 7.35 (ddd, J = 7.7, 1.3, 0.6 Hz, 1H), 7.46 (td, J = 7.6, 1.3 Hz, 1H), 7.65 (td, J = 7.6, 1.5 Hz, 1H), 7.77 (ddd, J = 7.7, 1.4, 0.5 Hz, 1H) ¹³C NMR δ 29.2, 34.0, 50.3, 54.3, 56.1, 60.0, 111.2, 114.0, (50 MHz, CDCl₃) 118.2, 122.2, 125.1, 126.0, 126.2, 128.1, 128.5, 128.8, 131.0, 132.8, 133.2, 140.3, 141.3, 145.3 ESI-MS m/z 385 ([M + H]⁺) EIHR-MS calcd for C₂₅H₂₅N₂O₂ [M + H]⁺, 385.1916; found, 385.1910 Compound number 38 Name 6-Methoxy-8-(2-nitrophenyl)-2-phenethyl-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.63-2.82 (m, 6H), 2.87-2.91 (m. 2H), 3.14 (d, J = (200 MHz, CDCl₃) 15.0 Hz, 1H), 3.40 (d, J = 14.9 Hz, 1H), 3.87 (s, 3H), 6.65 (s, 1H), 7.12-7.26 (m, 5H), 7.30-7.36 (m, 1H), 7.48-7.58 (m, 1H), 7.60-7.70 (m, 1H), 8.01- 8.08 (m, 1H) ¹³C NMR δ 28.9, 33.9, 50.3, 54.0, 56.1, 59.7, 110.6, 121.9, (50 MHz, CDCl₃) 124.6, 124.8, 125.8, 126.2, 128.5, 128.8, 131.0, 132.6, 133.1, 140.3, 140.7, 145.0, 149.6 ESI-MS m/z 405 ([M + H]⁺) EIHR-MS calcd for C₂₄H₂₅N₂O₄ [M + H]⁺, 405.1814; found, 405.1800 Compound number 39 Name 8-(2-Chlorophenyl)-6-methoxy-2-phenethyl- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.59-2.69 (m, 2H), 2.72-2.82 (m, 4H), 2.88-2.91 (200 MHz, CDCl₃) (m, 2H), 3.21 (d, J = 3.7 Hz, 2H), 3.85 (s, 3H), 6.65 (s, 1H), 7.11-7.22 (m, 6H), 7.28-7.33 (m 2H), 7.43- 7.52 (m, 1H) ¹³C NMR δ 29.1, 33.9, 50.4, 53.9, 56.0, 59.9, 110.5, 123.6, (50 MHz, CDCl₃) 125.4, 125.6, 126.0, 127.0, 128.4, 128.7, 129.1, 129.7, 131.5, 134.1, 134.9, 140.4, 141.1, 145.2 ESI-MS m/z 394 ([M + H]⁺) EIHR-MS calcd for C₂₄H₂₅ClNO₂ [M + H]⁺, 394.1574; found, 394.1571 Compound number 40 Name 8-(2-Acetylphenyl)-6methoxy-2-phenethyl-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.15 (s, 3H), 2.53-3.00 (m. 8H), 3.05 (d, J = 15.4 (200 MHz, CDCl₃) Hz, 1H), 3.28 (d, J = 15.1 Hz, 1H), 3.87 (s, 3H), 5.59 (bs, 1H), 6.65 (s, 1H), 7.06-7.61 (m, 8H), 7.76 (dd, J = 7.5, 1.6 Hz, 1H) ESI-MS m/z 402 ([M + H]⁺) EIHR-MS calcd for C₂₆H₂₈NO₃ [M + H]⁺, 402.2069; found, 402.2061 Compound number 41 Name 8-(2-Fluorophenyl)-6-methoxy-2-phenethyl-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.61-2.68 (m, 2H), 2.72-2.84 (m, 4H), 2.88-2.92 (200 MHz, CDCl₃) (m, 2H), 3.23 (d, J = 15.0 Hz, 1H), 3.37 (d, J = 15.0 Hz, 1H), 3.89 (s, 3H), 5.52 (s, 1H), 6.67 (s, 1H), 7.12-7.35 (m, 9H) ¹³C NMR δ 29.3, 34.0, 50.5, 54.3, 56.1, 60.1, 110.7, 115.9 (d, (50 MHz, CDCl₃) J = 22.3 Hz), 119.7, 123.1 (d, J = 17.7 Hz), 124.2, 125.6, 126.1, 128.4, 128.8, 129.7 (d, J = 7.9 Hz), 132.0, 140.1, 141.5, 145.2, 160.1 (d, J = 244 Hz) ESI-MS m/z 378.2 ([M + H]⁺) Compound number 42 Name (2-Methylphenyl)-6-methoxy-2-phenethyl-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.09 (s, 3H), 2.57-2.65 (m, 2H), 2.71-2.81 (m, (200 MHz, CDCl₃) 4H), 2.90-2.92 (m, 2H), 3.02 (d, J = 15.3 Hz, 1H), 3.25 (d, J = 15.2 Hz, 1H), 3.89 (s, 3H), 5.33 (s, 1H), 6.64 (s, 1H), 7.09-7.31 (m, 9H) ¹³C NMR δ 19.7, 29.4, 33.9, 50.6, 54.6, 56.1, 60.2, 110.0, (50 MHz, CDCl₃) 125.5, 125.6, 126.1, 128.0, 128.4, 128.8, 129.8, 130.3, 135.0, 137.0, 140.4, 140.7, 145.3 ESI-MS m/z 374.2 ([M + H]⁺) Compound number 43 Name 8-(2-Isopropylphenyl)-6-methoxy-2-phenethyl- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 1.12-1.17 (m, 3H), 1.26-1.30 (m, 3H), 2.65-2.94 (200 MHz, CDCl₃) (m, 8H), 3.12-3.20 (m, 2H), 3.63-3.65 (m, 1H), 3.91 (s, 3H), 5.30 (s, 1H), 6.67 (s, 1H), 7.06-7.42 (m, 9H) ¹³C NMR δ 24.0, 24.5, 29.3, 30.3, 33.9, 50.7, 54.7, 56.0, 60.2, (50 MHz, CDCl₃) 110.0, 125.5, 125.8, 126.1, 128.4, 128.7, 128.9, 129.9, 133.5, 140.3, 141.0, 145.2, 147.7 ESI-MS m/z 402.2 ([M + H]⁺) Compound number 44 Name 8-(3,5-Dimethoxyphenyl)-6-methoxy-2-phenethyl- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.58-2.72 (m, 2H), 2.73-2.82 (m, 4H), 2.93 (t, J = (200 MHz, CDCl₃) 3.0 Hz, 2H), 3.33 (s, 2H), 3.79 (s, 6H), 3.90 (s, 3H), 5.36 (s, 1H), 6.40 (s, 1H), 6.41 (s, 1H), 6.64 (s, 1H) 6.46-6.50 (m, 1H), 7.11-7.23 (m, 4H), 7.27-7.32 (m, 1H) ¹³C NMR δ 29.5, 34.1, 50.6, 54.8, 55.5, 56.2, 60.2, 100.0, (50 MHz, CDCl₃) 107.6, 110.3, 125.6, 126.1, 126.3, 128.5, 128.8, 137.5, 140.4, 140.8, 145.4, 161.0 ESI-MS m/z 420 ([M + H]⁺) EIHR-MS calcd for C₂₆H₃₀NO₄ [M + H]⁺, 420.2175; found, 420.2167 Compound number 45 Name 8-(2,3-Dimethoxyphenyl)-6-methoxy-2-phenethyl- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.54-2.86 (m, 6H), 2.87-3.00 (m, 2H), 3.28 (s, (200 MHz, CDCl₃) 2H), 3.62 (s, 3H), 3.89 (s, 3H), 3.90 (s, 3H), 5.46 (s, 1H), 6.65 (s, 1H), 6.73 (dd, J = 7.6, 1.5 Hz, 1H), 6.95 (dd, J = 8.2, 1.4 Hz, 1H), 7.07-7.29 (m, 6H) ¹³C NMR δ 29.3, 33.9, 50.6, 54.2, 55.8, 56.0, 60.0, 60.8, (50 MHz, CDCl₃) 110.2, 112.0, 122.6, 123.1, 124.3, 125.3, 126.0, 126.2, 128.4, 128.8, 129.7, 140.5, 140.9, 145.1, 147.0, 153.1 ESI-MS m/z 420 ([M + H]⁺) EIHR-MS calcd for C₂₆H₃₀NO₄ [M + H]⁺, 420.2175; found, 420.2159 Compound number 60 Name 8-Bromo-6-methoxy-2-phenethyl-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.70-3.01 (m, 8H), 3.64 (s, 2H), 3.86 (s, 3H), 6.58 (200 MHz, CDCl₃) (s, 1H), 7.17-7.37 (m, 5H) ¹³C NMR δ 29.3, 34.0, 50.4, 56.2, 56.4, 60.2, 109.0, 110.1, (50 MHz, CDCl₃) 126.2, 126.5, 127.3, 128.6, 128.9, 140.3, 141.2, 145.6 ESI-MS calcd for C₁₈H₂₁BrNO₂ m/z 362.1 EIHR-MS calcd for C₁₈H₂₁BrNO₂ [M + H]⁺, 362.0755; found, 362.0782 Compound number 61 Name 6-Methoxy-2-(2-(1-naphthyl)ethyl)-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.68-2.97 (m, 6H), 3.23-3.47 (m, 2H), 3.68 (s, (200 MHz, CDCl₃) 2H), 3.83 (s, 3H), 6.58 (s, 1H), 6.60 (s, 1H), 7.28- 7.58 (m, 4H), 7.64-7.91 (m, 2H), 8.00-8.17 (m, 1H) ¹³C NMR δ 28.8, 31.1, 51.3, 55.6, 56.0, 59.4, 110.8, 112.6, (50 MHz, CDCl₃) 123.9, 125.4, 125.6, 125.7, 126.1, 126.7, 127.0, 127.1, 128.9, 132.0, 134.0, 136.5, 144.0, 145.6 EIHR-MS calcd for C₂₂H₂₃NO₂ [M]⁺, 333.1729; found, 333.1721 Compound number 62 Name 2-(2-(3-indolyl)ethyl)-6-methoxy-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.76-2.94 (m, 6H), 3.00-3.15 (m, 2H), 3.66 (s, (200 MHz, CDCl₃) 2H), 3.85 (s, 3H), 6.59 (s, 1H), 6.61 (s, 1H), 7.02- 7.24 (m, 3H), 7.32-7.40 (m, 1H), 7.61-7.69 (m, 1H), 8.03 (s, 1H) ¹³C NMR δ 23.2, 28.7, 51.1, 55.5, 55.9, 58.9, 110.7, 111.1, (50 MHz, CDCl₃) 112.3, 114.4, 118.8, 119.2, 121.5, 121.9, 125.5, 127.3, 127.5, 136.2, 143.7, 145.3 EIHR-MS calcd for C₂₀H₂₂N₂O₂ [M]⁺, 322.1681; found, 322.1675 Compound number 63 Name 6-Methoxy-2-(2-nitrophenethyl)-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.78-2.86 (m, 6H), 3.16-3.23 (m, 2H), 3.63 (s, (200 MHz, CDCl₃) 2H), 3.85 (s, 3H), 6.58 (m, 1H), 6.59 (s, 1H), 7.36- 7.44 (m, 2H), 7.49-7.53 (m, 1H), 7.92 (dd, J = 8.1, 1.3 Hz, 1H) ¹³C NMR δ 28.9, 31.0, 50.9, 55.5, 56.1, 58.8, 110.8, 112.4, (50 MHz, CDCl₃) 125.6, 127.4, 132.7, 133.2, 135.5, 143.8, 145.4, 149.6 ESI-MS m/z 329.2 ([M + H]⁺), 351.1 ([M + Na]⁺) Compound number 64 Name 6-Methoxy-2-(3-nitrophenethyl)-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.73-2.89 (m, 6H), 2.95-3.03 (m, 2H), 3.58 (s, (200 MHz, CDCl₃) 2H), 3.82 (s, 1H), 5.73 (s, 1H), 6.55 (s, 2H), 7.42 (t, J = 7.8 Hz, 1H), 7.52, (d, J = 7.6 Hz, 1H), 8.03-809 (m, 2H) ¹³C NMR δ 28.8, 33.6, 51.2, 55.6, 56.1, 59.4, 110.8, 112.4, (50 MHz, CDCl₃) 121.4, 123.7, 125.5, 127.0, 129.4, 135.3, 142.5, 143.9, 145.5, 148.4 ESI-MS m/z 329.2 ([M + H]⁺), 351.1 ([M + Na]⁺) Compound number 65 Name 6-Methoxy-2-(4-nitrophenethyl)-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.74-2.86 (m, 6H), 2.97-3.04 (m, 2H), 3.60 (s, (200 MHz, CDCl₃) 2H), 3.85 (s, 3H), 6.57 (s, 2H), 7.36-7.43 (m, 2H), 8.11-8.18 (m, 2H) ¹³C NMR δ 28.8, 33.9, 51.2, 55.6, 56.1, 59.3, 110.8, 112.4, (50 MHz, CDCl₃) 123.8, 125.5, 127.0, 129.7, 143.9, 145.5, 146.6, 148.5 ESI-MS ESIMS m/z 329.1 ([M + H]⁺) Compound number 66 Name 2-(4-Chlorophenethyl)-6-methoxy-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.66-2.93 (m, 8H), 3.58 (s, 2H), 3.83 (s, 3H), 6.54 (200 MHz, CDCl₃) (s, 1H), 6.56 (s, 1H), 7.11-7.19 (m, 2H), 7.21-7.28 (m, 2H) ¹³C NMR δ 28.7, 33.3, 51.2, 55.5, 56.0, 60.0, 110.8, 112.5, (50 MHz, CDCl₃) 125.4, 127.0, 128.6, 130.2, 131.9, 138.9, 143.9, 145.5 EIHR-MS calcd for C₁₈H₂₀ClNO₂ [M]⁺, 317.1183; found, 317.1180 Compound number 67 Name 2-(2,4-Dichlorophenethyl)-6-methoxy-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.63-2.91 (m, 8H), 3.61 (s, 2H), 3.83 (s, 3H), 6.56 (200 MHz, CDCl₃) (s, 2H), 7.15-7.24 (m, 2H), 7.33-7.43 (m, 1H) ¹³C NMR δ 28.8, 31.0, 51.0, 55.5, 56.0, 57.8, 110.8, 112.5, (50 MHz, CDCl₃) 125.5, 127.1, 127.2, 129.3, 131.7, 132.6, 134.8, 136.6, 143.9, 145.4 EIHR-MS calcd for C₁₈H₁₉Cl₂NO₂ [M]⁺, 351.0793; found, 351.0799 Compound number 68 Name 2-(4-Bromophenethyl)-6-methoxy-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.67-2.92 (m, 8H), 3.59 (s, 2H), 3.84 (s, 3H), 6.57 (200 MHz, CDCl₃) (s, 2H), 7.07-7.15 (m, 2H), 7.37-7.44 (m, 2H) ¹³C NMR δ 28.8, 33.5, 51.2, 55.6, 56.1, 60.0, 110.8, 112.4, (50 MHz, CDCl₃) 120.0, 125.5, 127.2, 130.6, 130.6, 139.5, 143.9, 145.4 EIHR-MS calcd for C₁₈H₂₀BrNO₂ [M]⁺, 313.0677; found, 313.0676 Compound number 69 Name 2-(3-Bromophenethyl)-6-methoxy-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.67-2.93 (m, 8H), 3.59 (s, 2H), 3.84 (s, 3H), 6.57 (200 MHz, CDCl₃) (s, 2H), 7.13-7.19 (m, 2H), 7.28-7.40 (m, 2H) ¹³C NMR δ 28.8, 33.7, 51.2, 55.6, 56.1, 60.0, 110.8, 112.4, (50 MHz, CDCl₃) 122.5, 125.5, 127.2, 127.6, 129.3, 130.1, 131.9, 142.9, 143.9, 145.4 EIHR-MS calcd for C₁₈H₂₀BrNO₂ [M]⁺, 313.0677; found, 313.0665 Compound number 70 Name 6-Methoxy-2-(3-Methoxyphenethyl)-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.69-2.96 (m, 8H), 3.60 (s, 2H), 3.80 (s, 3H), 3.84 (200 MHz, CDCl₃) (s, 3H), 6.57 (s, 2H), 6.72-6.88 (m, 3H), 7.16-7.28 (m, 1H) ¹³C NMR δ 28.8, 34.1, 51.2, 55.3, 55.6, 56.1, 60.3, 110.8, (50 MHz, CDCl₃) 111.5, 112.1, 112.4, 114.6, 121.2, 125.5, 127.2, 129.5, 142.1, 143.8, 145.4, 159.7 EIHR-MS calcd for C₁₉H₂₃NO₃ [M]⁺, 313.1678; found, 313.1678 Compound number 71 Name 2-Heptyl-6-methoxy-1,2,3,4-tetrahydroisoquinolin- 7-ol ¹H NMR δ 0.85-0.88 (m, 3H), 1.18-1.50 (m, 8H), 1.50-1.70 (200 MHz, CDCl₃) (m, 2H), 2.43-2.51 (m, 2H), 2.66-2.71 (m, 2H), 2.78-2.81 (m, 2H), 3.50 (s, 2H), 3.83 (s, 3H), 6.55 (s, 2H) ¹³C NMR δ 14.2, 22.8, 27.3, 27.8, 28.8, 29.4, 32.0, 51.2, 55.7, (50 MHz, CDCl₃) 56.0, 58.7, 110.8, 112.5, 125.6, 127.6, 143.8, 145.4 ESI-MS m/z 278.2 ([M + H]⁺) Compound number 72 Name 6-Methoxy-2-octyl-1,2,3,4-tetrahydroisoquinolin-7- ol ¹H NMR δ 0.88 (s, 3H), 1.18-1.50 (m, 10H), 1.50-1.70 (m, (200 MHz, CDCl₃) 2H), 2.43-2.51 (m, 2H), 2.66-2.71 (m, 2H), 2.78- 2.81 (m, 2H), 3.50 (s, 2H), 3.84 (s, 3H), 6.56 (s, 2H) ¹³C NMR δ 14.3, 22.8, 27.3, 27.8, 28.8, 29.4, 29.7, 32.0, 51.2, (50 MHz, CDCl₃) 55.8, 56.1, 58.7, 110.8, 112.5, 125.6, 127.5, 143.8, 145.4 ESI-MS m/z 292.2 ([M + H]⁺) Compound number 73 Name 6-Methoxy-2-nonyl-1,2,3,4-tetrahydroisoquinolin- 7-ol ¹H NMR δ 0.88 (s, 3H), 1.28 (bs, 12H), 1.50-1.70 (m, 2H), (200 MHz, CDCl₃) 2.43-2.51 (m, 2H), 2.69-2.72 (m, 2H), 2.79-2.81 (m, 2H), 3.50 (s, 2H), 3.83 (s, 3H), 6.55 (s, 2H) ¹³C NMR δ 14.3, 22.8, 27.3, 27.8, 28.8, 29.4, 29.7, 32.0, 51.2, (50 MHz, CDCl₃) 55.7, 56.1, 58.7, 110.8, 112.5, 125.7, 127.5, 143.8, 145.4 ESI-MS m/z 306.2 ([M + H]⁺) Compound number 74 Name 2-(3,4-Dimethoxyphenethyl)-6-methoxy-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.68-2.93 (m, 8H), 3.60 (s, 2H), 3.84 (s, 3H), 3.86 (200 MHz, CDCl₃) (s, 3H), 3.87 (s, 3H), 6.57 (s, 2H), 6.73-6.84 (m, 3H) ¹³C NMR δ 28.8, 33.6, 51.3, 55.6, 56.0, 60.5, 110.8, 111.3, (50 MHz, CDCl₃) 112.1, 112.4, 120.6, 125.5, 127.2, 133.0, 143.8, 145.4, 147.4, 148.9 EIHR-MS calcd for C₂₀H₂₅NO₄ [M]⁺, 343.1784; found, 343.1788 Compound number 75 Name 2-(2-Chlorophenethyl)-6-methoxy-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.68-2.90 (m, 6 H), 2.98-3.11 (m, 2H), 3.63 (s, (200 MHz, CDCl₃) 2H), 3.83 (s, 3H), 6.57 (s, 2H), 7.09-7.24 (m, 2H), 7.24-7.39 (m, 2H) ¹³C NMR δ 28.8, 31.6, 51.0, 55.5, 56.0, 58.1, 110.8, 112.5, (50 MHz, CDCl₃) 125.5, 127.0, 127.2, 127.7, 129.6, 131.0, 134.1, 138.0, 143.8, 145.4 ESI-MS m/z 318 ([M + H]⁺), 340 ([M + Na]⁺) EIHR-MS calcd for C₁₈H₂₁ClNO₂ [M + H]⁺, 318.1261; found, 318.1253 Compound number 76 Name 2-(2-Fluorophenethyl)-6-methoxy-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.68-2.89 (m, 6H), 2.89-3.01 (m, 2H), 3.61 (s, (200 MHz, CDCl₃) 2H), 3.83 (s, 3H), 6.56 (s, 2H), 6.94-7.11 (m, 2H), 7.12-7.30 (m, 2H) ¹³C NMR δ 27.2, 28.8, 51.1, 55.5, 56.0, 58.6, 110.8, 112.5, (50 MHz, CDCl₃) 115.4 (J = 22.1 Hz), 124.1 (J = 3.1 Hz), 125.5, 127.2 (J = 15.9 Hz), 127.3, 127.9 (J = 7.9 Hz), 131.1 (J = 4.8 Hz), 143.8, 145.4, 161.3 (J = 243 Hz) ESI-MS m/z 302 ([M + H]⁺) EIHR-MS calcd for C₁₈H₂₁FNO₂ [M + H]⁺, 302.1556; found, 302.1554 Compound number 77 Name 6-Methoxy-2-(3-(4-nitrophenyl)propyl)-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 1.84-2.05 (m, 2H), 2.44-2.56 (m, 2H), 2.63-2.74 (200 MHz, CDCl₃) (m, 2H), 2.74-2.88 (m, 4H), 3.50 (s, 2H), 3.83 (s, 3H), 6.54 (s, 1H), 6.56 (s, 1H), 7.30-7.42 (m, 2H), 8.09-8.20 (m, 2H) ¹³C NMR δ 28.4, 28.8, 33.6, 51.2, 55.6, 56.0, 57.3, 110.8, (50 MHz, CDCl₃) 112.4, 123.7, 125.5, 127.2, 129.4, 143.8, 145.4, 146.4, 150.3 EIHR-MS calcd for C₁₉H₂₃N₂O₄ [M + H]⁺, 343.1658; found, 343.1661 Compound number 78 Name 6-Methoxy-2-(3-(2-nitrophenyl)propyl)-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 1.80-2.09 (m, 2H), 2.44-2.63 (m, 2H), 2.64-2.75 (200 MHz, CDCl₃) (m, 2H), 2.76-2.88 (m, 2H), 2.88-3.07 (m, 2H), 3.51 (s, 2H), 3.83 (s, 3H), 6.55 (s, 1H), 6.56 (s, 1H), 7.28-7.43 (m, 2H), 7.45-7.58 (m, 1H), 7.83-7.95 (m, 1H) ¹³C NMR δ 28.2, 28.8, 31.0, 51.0, 55.7, 56.0, 57.7, 110.8, (50 MHz, CDCl₃) 112.4, 124.8, 125.6, 127.1, 127.4, 132.2, 133.0, 137.4, 143.8, 145.4, 149.5 EIHR-MS calcd for C₁₉H₂₃N₂O₄ [M + H]⁺, 343.1658; found, 343.1661 Compound number 85 Name 8-Bromo-6-methoxy-2-(4-nitrophenethyl)-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.71-2.93 (m, 6H), 2.97-3.10 (m, 2H), 3.62 (s, (200 MHz, CDCl₃) 2H), 3.87 (s, 3H), 6.59 (s, 1H), 7.37-7.46 (m, 2H), 8.12-8.20 (m, 2H) ¹³C NMR δ 29.3, 33.9, 50.4, 56.1, 56.4, 59.1, 108.8, 110.1, (50 MHz, CDCl₃) 123.8, 126.2, 127.1, 129.7, 141.3, 145.6, 146.6, 148.4 ESI-MS m/z 407 ([M + H]⁺), 429 ([M + Na]⁺) EIHR-MS calcd for C₁₈H₂₀BrN₂O₄ [M + H]⁺, 407.0606; found, 407.0585 Compound number 95 Name 8-Bromo-2-(2-chlorophenethyl)-6-methoxy-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.72-2.93 (m, 6H), 2.98-3.15 (m, 2H), 3.66 (s, (200 MHz, CDCl₃) 2H), 3.86 (s, 3H), 6.11 (bs, 1H), 6.58 (s, 1H), 7.10- 7.25 (m, 2H), 7.25-7.41 (m, 2H) ¹³C NMR δ 29.4, 31.6, 50.2, 56.2, 56.4, 58.0, 108.9, 110.2, (50 MHz, CDCl₃) 126.6, 127.0, 127.3, 127.8, 129.7, 131.0, 134.2, 138.0, 141.2, 145.5 ESI-MS m/z 396 ([M + H]⁺) EIHR-MS calcd for C₁₈H₂₀BrClNO₂ [M + H]⁺, 396.0366; found, 396.0355 Compound number 96 Name 8-Bromo-2-(2-fluorophenethyl)-6-methoxy-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.69-2.91 (m, 6H), 2.91-3.05 (m, 2H), 3.63 (s, (200 MHz, CDCl₃) 2H), 3.85 (s, 3H), 6.57 (s, 1H), 6.94-7.12 (m, 2H), 7.12-7.33 (m, 2H) ¹³C NMR δ 27.2, 29.3, 50.2, 56.2, 56.4, 58.4, 109.1, 110.2, (50 MHz, CDCl₃) 115.4 (J = 21.9 Hz), 124.1 (J = 3.2 Hz), 126.5, 127.0, 127.2, 128.0 (J = 8.1 Hz), 131.1 (J = 5.0 Hz), 141.2, 145.6, 161.3 (J = 243 Hz) ESI-MS m/z 380 ([M + H]⁺) EIHR-MS calcd for C₁₈H₂₀BrFNO₂ [M + H]⁺, 380.0661; found, 380.0662 Compound number 97 Name 8-Bromo-6-methoxy-2-(3-(4-nitrophenyl)propyl)- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 1.87-2.06 (m, 2H), 2.49-2.74 (m, 4H), 2.74-2.90 (200 MHz, CDCl₃) (m, 4H), 3.53 (s, 2H), 3.85 (s, 3H), 6.57 (s, 1H), 7.31-7.43 (m, 2H), 8.07-8.21 (m, 2H) ¹³C NMR δ 28.4, 29.3, 33.6, 50.4, 56.2, 56.4, 57.2, 109.0, (50 MHz, CDCl₃) 110.1, 123.8, 126.4, 127.2, 129.4, 141.3, 145.6, 146.4, 150.2 ESI-MS m/z 421 ([M + H]⁺) EIHR-MS calcd for C₁₉H₂₂BrN₂O₄ [M + H]⁺, 421.0763; found, 421.0757 Compound number 98 Name 8-Bromo-6-methoxy-2-(3-(2-nitrophenyl)propyl)- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 1.86-2.11 (m, 2H), 2.51-2.75 (m, 4H), 2.75-2.90 (200 MHz, CDCl₃) (m, 2H), 2.90-3.06 (m, 2H), 3.53 (s, 2H), 3.83 (s, 3H), 6.55 (s, 1H), 7.31-7.43 (m, 2H), 7.45-7.58 (m, 1H), 7.82-7.94 (m, 1H) ¹³C NMR δ 28.1, 29.2, 30.9, 50.1, 56.3, 57.5, 109.1, 110.1, (50 MHz, CDCl₃) 124.8, 126.5, 127.1, 127.3, 132.1, 133.0, 137.3, 141.2, 145.7, 149.4 ESI-MS m/z 421 ([M + H]⁺) Compound number 101 Name 8-(2,4-Dimethoxyphenyl)-6-methoxy-2-(2-(1- naphthyl)ethyl)-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.69-3.02 (m, 6H), 3.19-3.37 (m, 4H), 3.73 (s, (200 MHz, CDCl₃) 3H), 3.82-3.93 (m, 6H), 6.54-6.63 (m, 1H), 6.63- 6.72 (m, 1H), 7.03-7.12 (m, 1H), 7.25-7.29 (m, 1H), 7.29-7.35 (m, 1H), 7.35-7.43 (m, 1H), 7.43-7.55 (m, 2H), 7.65-7.76 (m, 1H), 7.79-7.89 (m, 1H), 7.95-8.04 (m, 1H) ¹³C NMR δ 29.2, 31.1, 50.7, 54.3, 55.5, 55.8, 56.1, 59.2, 99.2, (50 MHz, CDCl₃) 104.9, 110.3, 116.3, 122.6, 123.9 (×2), 125.1, 125.6, 125.7, 126.0, 126.7, 127.0, 128.9, 132.0 (×2), 134.0, 136.6, 141.5, 145.4, 158.2, 160.9 Compound number 102 Name 8-(2,4-Dimethoxyphenyl)-2-(2-(3-indolyl)ethyl)-6- methoxy-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.72-3.42 (m, 10H), 3.70 (s, 3H), 3.85 (s, 3H), (200 MHz, CDCl₃) 3.88 (s, 3H), 6.53-6.70 (m, 2H), 6.73-6.87 (m, 1H), 6.94-7.23 (m, 5H), 7.28-7.40 (m, 1H), 7.51-7.69 (m, 1H) Compound number 105 Name 8-(2,4-Διμετηοξψπηενψλ)-6-μετηοξψ-2-(4-νιτρο πηενετηψλ)-1,2,3,4-τετραηψδροισοθυινολιν-7-ολ ¹H NMR δ 2.61-2.81 (m, 4H), 2.82-2.95 (m, 4H), 3.23 (s, (200 MHz, CDCl₃) 2H), 3.72 (s, 3H), 3.85 (s, 3H), 3.88 (s, 3H), 6.53- 6.61 (m, 2H), 6.63 (s, 1H), 6.91-7.17 (m, 1H), 7.25- 7.35 (m, 2H), 8.05-8.13 (m, 2H) ¹³C NMR δ 29.3, 33.7, 50.7, 54.2, 55.5, 55.7, 56.0, 59.1, 99.2, (50 MHz, CDCl₃) 104.8, 110.2, 116.3, 122.4, 123.7, 125.0, 126.4, 129.6, 131.9, 141.4, 145.2, 146.5, 148.6, 158.1, 160.8 EIHR-MS calcd for C₂₆H₂₉N₂O₆ [M + H]⁺, 465.2025; found, 465.2055 Compound number 106 Name 2-(4-Chlorophenethyl)-8-(2,4-dimethoxyphenyl)-6- methoxy-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.47-2.77 (m, 6H), 2.77-2.88 (m, 2H), 3.16 (s, (200 MHz, CDCl₃) 2H), 3.65 (s, 3H), 3.78 (s, 3H), 3.80 (s, 3H), 6.47- 6.54 (m, 2H), 6.55 (s, 1H), 6.93-7.05 (m, 3H), 7.09- 7.20 (m, 2H) ¹³C NMR δ 29.3, 33.3, 50.6, 54.2, 55.4, 55.7, 56.0, 59.8, 99.2, (50 MHz, CDCl₃) 104.8, 110.2, 116.3, 122.5, 125.1, 126.6, 128.5, 130.1, 131.7, 131.9, 139.0, 141.4, 145.2, 158.1, 160.7 ESI-MS m/z 452 ([M − H]⁺), 476 ([M + Na]⁺) EIHR-MS calcd for C₂₆H₂₇ClNO₄ [M − H⁺], 452.1629; found, 452.1623 Compound number 107 Name 2-(2,4-Dichlorophenethyl)-8-(2,4- dimethoxyphenyl)-6-methoxy-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.54-2.65 (m, 2H), 2.69-2.95 (m, 6H), 3.26 (s, (200 MHz, CDCl₃) 2H), 3.73 (s, 3H), 3.85 (s, 3H), 3.88 (s, 3H), 6.54- 6.61 (m, 2H), 6.63 (s, 1H), 7.02-7.07 (m, 1H), 7.12 (s, 1H), 7.12 (s, 1H), 7.30-7.33 (m, 1H) ESI-MS m/z 488 ([M + H]⁺) EIHR-MS calcd for C₂₆H₂₆Cl₂NO₄ [M − H]⁺, 486.1239; found, 486.1233 Compound number 108 Name 2-(4-Bromophenethyl)-8-(2,4-dimethoxyphenyl)-6- methoxy-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.53-2.83 (m, 6H), 2.84-2.96 (m, 2H), 3.23 (bd, (200 MHz, CDCl₃) 2H), 3.72 (s, 3H), 3.85 (s, 3H), 3.87 (s, 3H), 6.53- 6.62 (m, 2H), 6.62 (s, 1H), 6.98-7.07 (m, 3H), 7.28- 7.42 (m, 2H) ¹³C NMR δ 29.3, 33.4, 50.6, 54.2, 55.5, 55.7, 56.0, 59.7, 99.2, (50 MHz, CDCl₃) 104.8, 110.2, 116.3, 119.8, 122.5, 125.1, 126.6, 130.6, 131.4, 131.9, 139.6, 141.4, 145.3, 158.2, 160.8 ESI-MS m/z 496 ([M − H]⁺) EIHR-MS calcd for C₂₆H₂₇BrNO₄ [M − H]⁺, 496.1123; found, 496.1118 Compound number 109 Name 2-(3-Bromophenethyl)-8-(2,4-dimethoxyphenyl)-6- methoxy-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.54-2.83 (m, 6H), 2.83-2.96 (m, 2H), 3.13-3.33 (200 MHz, CDCl₃) (m, 2H), 3.72 (s, 3H), 3.85 (s, 3H), 3.87 (s, 3H), 6.54-6.61 (m, 2H), 6.62 (s, 1H), 6.99-7.15 (m, 3H), 7.24-7.35 (m, 1H) ¹³C NMR δ 29.2, 33.6, 50.6, 54.2, 55.4, 55.7, 56.0, 59.6, 99.2, (50 MHz, CDCl₃) 110.2, 116.3, 122.4, 122.5, 125.0, 126.5, 127.5, 129.1, 130.7, 131.7, 131.9, 141.4, 142.9, 145.2, 158.1, 160.8 ESI-MS m/z 498 ([M + H]⁺) EIHR-MS calcd for C₂₆H₂₇BrNO₄ [M − H]⁺, 496.1123; found, 496.1118 Compound number 110 Name 8-(2,4-Dimethoxyphenyl)-6-methoxy-2-(3- methoxyphenethyl)-1,2,3,4-tetrahydroisoquinolin- 7-ol ¹H NMR δ 2.51-2.85 (m, 6H), 2.86-2.98 (m, 2H), 3.25 (s, (200 MHz, CDCl₃) 2H), 3.71 (s, 3H), 3.76 (s, 3H), 3.84 (s, 3H), 3.86 (s, 3H), 6.53-6.60 (m, 2H), 6.62 (s, 1H), 6.67-6.79 (m, 3H), 7.00-7.07 (m, 1H), 7.10-7.21 (m, 1H) ¹³C NMR δ 29.2, 33.9, 50.5, 54.1, 55.2, 55.4, 55.6, 55.9, 59.9, (50 MHz, CDCl₃) 99.1, 104.8, 110.1, 111.3, 114.4, 116.3, 121.1, 122.4, 125.0, 126.5, 129.3, 131.8, 141.3, 142.0, 145.2, 158.0, 159.6, 160.7 ESI-MS m/z 448 ([M − H]⁺), 472 ([M + Na]⁺) EIHR-MS calcd for C₂₇H₃₁NO₅ [M]⁺, 449.2202; found, 449.2197 Compound number 111 Name 8-(2,4-Dimethoxyphenyl)-2-heptyl-6-methoxy- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 0.83-0.89 (m, 3H), 1.10-1.39 (m, 8H), 1.40-1.45 (200 MHz, CDCl₃) (m, 2H), 2.31-2.38 (m, 2H), 2.63-2.71 (m, 2H), 2.85-2.91 (m, 2H), 3.16 (s, 2H), 3.73 (s, 3H), 3.86 (s, 3H), 3.87 (s, 3H), 5.30 (s, 1H), 6.46-6.61 (m, 2H), 6.67 (d, J = 8.4 Hz, 1H), 7.02-7.06 (m, 1H) ¹³C NMR δ 14.2, 22.8, 27.3, 27.7, 29.4, 32.0, 50.5, 54.5, 55.5, (50 MHz, CDCl₃) 55.7, 56.0, 58.5, 99.2, 104.8, 110.2, 125.3, 132.0, 141.3, 145.1, 158.2, 160.8 ESI-MS m/z 414.3 ([M + H]⁺) Compound number 112 Name 8-(2,4-Dimethoxyphenyl)-6-methoxy-2-octyl- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 0.83-0.89 (m, 3H), 1.10-1.38 (m, 10H), 1.40-1.55 (200 MHz, CDCl₃) (m, 2H), 2.31-2.38 (m, 2H), 2.63-2.71 (m, 2H), 2.85-2.91 (m, 2H), 3.16 (s, 2H), 3.73 (s, 3H), 3.86 (s, 3H), 3.87 (s, 3H), 5.30 (s, 1H), 6.55-6.61 (m, 2H), 6.67 (d, J = 8.4 Hz, 1H), 7.02-7.06 (m, 1H) ¹³C NMR δ 14.2, 22.8, 27.2, 27.7, 29.4 (×2), 29.6, 31.9, 50.5, (50 MHz, CDCl₃) 54.4, 55.5, 55.7, 56.0, 58.4, 99.2, 104.8, 110.2, 125.3, 126.9, 132.0, 141.4, 145.2, 158.2 ESI-MS m/s 428.3 ([M + H]⁺) Compound number 113 Name 8-(2,4-Dimethoxyphenyl)-6-methoxy-2-nonyl- 1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 0.84-0.90 (m, 3H), 1.24 (bs, 12H), 1.40-1.55 (m, (200 MHz, CDCl₃) 2H), 2.31-2.38 (m, 2H), 2.61-2.71 (m, 2H), 2.85- 2.91 (m, 2H), 3.16 (s, 2H), 3.73 (s, 3H), 3.86 (s, 3H), 3.87 (s, 3H), 5.29 (s, 1H), 6.55-6.61 (m, 2H), 6.67 (d, J = 8.4 Hz, 1H), 7.02-7.06 (m, 1H) ¹³C NMR δ 14.2, 22.8, 27.2, 27.7, 29.4, 29.7, 32.0, 50.5, 54.5, (50 MHz, CDCl₃) 55.5, 55.7, 56.0, 58.4, 99.2, 104.8, 110.2, 122.5, 125.3, 127.0, 131.9, 141.4, 145.2, 158.2, 160.7 ESI-MS m/z 442.3 ([M + H]⁺) Compound number 114 Name 2-(3,4-Dimethoxyphenethyl)-8-(2,4- dimethoxyphenyl)-6-methoxy-1,2,3,4- tetrahydroisoquinolin-7-ol ¹H NMR δ 2.54-2.84 (m, 6H), 2.85-2.97 (m, 2H), 3.26 (bd, (200 MHz, CDCl₃) 2H), 3.71 (s, 3H), 3.83 (s, 3H), 3.83 (s, 6H), 3.86 (s, 3H), 6.53-6.60 (m, 2H), 6.62 (s, 1H), 6.65-6.79 (m, 3H), 7.00-7.07 (m, 1H) ¹³C NMR δ 29.2, 33.5, 50.5, 54.1, 55.3, 55.6, 55.8, 55.9, 60.1, (50 MHz, CDCl₃) 99.0, 104.7, 110.1, 111.1, 111.9, 116.3, 120.5, 122.4, 125.0, 126.5, 131.8, 133.0, 141.3, 145.1, 147.2, 148.7, 158.0, 160.6 ESI-MS m/z 478 ([M − H]⁺), 502 ([M + Na]⁺) EIHR-MS calcd for C₂₈H₃₃NO₆ [M]⁺, 479.2308; found, 479.2302 Compound number 115 Name 2-(2-Chlorophenethyl)-8-(2,4-dimethoxyphenyl)-6- methoxy-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.48-2.60 (m, 2H), 2.63-2.93 (m, 6H), 3.20 (s, (200 MHz, CDCl₃) 2H), 3.63 (s, 3H), 3.75 (s, 3H), 3.77 (s, 3H), 6.44- 6.52 (m, 2H), 6.54 (s, 1H), 6.92-7.14 (m, 4H), 7.15- 7.25 (m, 1H) ¹³C NMR δ 29.2, 31.5, 50.4, 54.2, 55.4, 55.6, 55.9, 57.9, 99.1, (50 MHz, CDCl₃) 104.7, 110.1, 116.3, 122.5, 125.0, 126.7, 126.8, 127.5, 129.4, 130.8, 131.9, 134.0, 138.0, 141.4, 145.2, 158.1, 160.7 EIHR-MS calcd for C₂₆H₂₉ClNO₄ [M + H]⁺, 454.1785; found, 454.1799 Compound number 116 Name 8-(2,4-Dimethoxyphenyl)-2-(2-fluorophenethyl)-6- methoxy-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.55-2.95 (m, 8H), 3.26 (s, 2H), 3.72 (s, 3H), 3.84 (200 MHz, CDCl₃) (s, 3H), 3.87 (s, 3H), 6.53-6.61 (m, 2H), 6.62 (s, 1H), 6.89-7.22 (m, 5H) ¹³C NMR δ 27.1, 29.2, 50.4, 54.2, 55.4, 55.7, 56.0, 58.3, 99.2, (50 MHz, CDCl₃) 104.8, 110.2, 115.2 (J = 22.0 Hz), 116.3, 122.5, 124.0 (J = 3.0 Hz), 125.1, 126.7, 127.3 (J = 16.0 Hz), 127.8 (J = 7.9 Hz), 131.0 (J = 4.9 Hz), 131.9, 141.3, 145.2, 158.1, 160.8, 161.2 (J = 243 Hz) EIHR-MS calcd for C₂₆H₂₉FNO₄ [M + H]⁺, 438.2081; found, 438.2099 Compound number 119 Name 8-(2,4-Dimethoxyphenyl)-2-(4-fluorophenethyl)-6- methoxy-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.54-2.82 (m, 6H), 2.85-2.96 (m, 2H), 3.24 (d, J = (200 MHz, CDCl₃) 2.1 Hz, 2H), 3.71 (s, 3H), 3.84 (s, 3H), 3.86 (s, 3H), 6.53-6.60 (m, 2H), 6.62 (s, 1H), 6.84-6.97 (m, 2H), 7.00-7.14 (m, 3H) ¹³C NMR δ 29.3, 33.3, 50.7, 54.3, 55.5, 55.8, 56.1, 60.1, 99.3, (50 MHz, CDCl₃) 104.9, 110.3, 115.0, 115.4, 116.4, 122.7, 125.1, 126.6, 130.1, 130.3, 132.0, 136.2, 141.6, 145.4, 158.2, 160.9, 161.5 (d, J = 242 Hz) Compound number 120 Name 8-(2,4-Dimethoxyphenyl)-6-methoxy-2-(4-meth- oxyphenethyl)-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.54-2.80 (m, 6H), 2.84-2.93 (m, 2H), 3.25 (s, (200 MHz, CDCl₃) 2H), 3.71 (s, 3H), 3.76 (s, 3H), 3.84 (s, 3H), 3.87 (s, 3H), 6.54-6.60 (m, 2H), 6.62 (s, 1H), 6.75-6.83 (m, 2H), 7.01-7.11 (m, 3H) ¹³C NMR δ 29.3, 33.1, 50.6, 54.2, 55.3, 55.4, 55.7, 56.0, 60.4, (50 MHz, CDCl₃) 99.1, 104.8, 110.2, 113.8, 116.4, 122.5, 125.1, 126.7, 129.6, 131.9, 132.6, 141.4, 145.2, 157.9, 158.1, 160.7 ESI-MS m/z 448 ([M − H]⁺), 472 ([M + Na]⁺) EIHR-MS calcd for C₂₇H₃₁NO₅ [M]⁺, 448.2124; found, 448.2118 Compound number 121 Name 8-(2,4-Dimethoxyphenyl)-6-methoxy-2-(4-meth- ylphenethyl)-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.29 (s, 3H), 2.55-2.84 (m, 6H), 2.84-2.96 (m, (200 MHz, CDCl₃) 2H), 3.25 (bd, 2H), 3.71 (s, 3H), 3.84 (s, 3H), 3.86 (s, 3H), 6.54-6.60 (m, 2H), 6.62 (s, 1H), 7.01 (s, 1H), 7.02-7.07 (m, 4H) ¹³C NMR δ 21.1, 29.3, 33.5, 50.6, 54.2, 55.4, 55.7, 56.0, 60.2, (50 MHz, CDCl₃) 99.1, 104.8, 110.2, 116.4, 122.5, 125.1, 126.7, 128.6, 129.0, 131.9, 135.5, 137.4, 141.4, 145.2, 158.1, 160.7 EIHR-MS calcd for C₂₇H₃₂NO₄ [M + H]⁺, 434.2331; found, 434.2348 Compound number 122 Name 2-(3-Chlorophenethyl)-8-(2,4-dimethoxyphenyl)-6- methoxy-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.58-2.99 (m, 8H), 3.12 (d, J = 15.4 Hz, 1H), 3.20 (200 MHz, CDCl₃) (d, J = 15.3 Hz, 1H), 3.65 (s, 3H), 3.78 (s, 3H), 3.80 (s, 3H), 6.46-6.54 (m, 2H), 6.55 (s, 1H), 6.91-7.01 (m, 2H), 7.03-7.14 (m, 3H) ¹³C NMR δ 29.2, 33.7, 50.6, 54.2, 55.4, 55.7, 56.0, 59.6, 99.2, (50 MHz, CDCl₃) 104.8, 110.1, 116.3, 122.5, 125.0, 126.2, 126.5, 127.0, 128.8, 129.6, 131.9, 134.1, 141.4, 142.5, 145.2, 158.1, 160.8 EIHR-MS calcd for C₂₆H₂₉ClNO₄ [M + H]⁺, 454.1785; found, 454.1798 Compound number 123 Name 8-(2,4-Dimethoxyphenyl)-6-methoxy-2-(2-meth- oxyphenethyl)-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 2.52-2.86 (m, 6H), 2.87-2.98 (m, 2H), 3.27 (s, (200 MHz, CDCl₃) 2H), 3.71 (s, 3H), 3.75 (s, 3H), 3.83 (s, 3H), 3.86 (s, 3H), 6.53-6.61 (m, 2H), 6.62 (s, 1H), 6.76-6.89 (m, 2H), 7.01-7.19 (m, 3H) ¹³C NMR δ 28.1, 29.3, 50.3, 54.2, 55.2, 55.4, 55.6, 58.3, 99.1, (50 MHz, CDCl₃) 104.7, 104.7, 110.1, 110.3, 116.4, 120.4, 122.5, 125.2, 126.9, 127.3, 128.8, 130.2, 131.9, 141.3, 145.1, 157.5, 158.1, 160.7 EIHR-MS calcd for C₂₇H₃₂NO₅ [M + H]⁺, 450.2280; found, 450.2297 Compound number 125 Name 8-(2,4-Dimethoxyphenyl)-6-methoxy-2-(3- phenylpropyl)-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 1.70-1.88 (m, 2H), 2.35-2.47 (m, 2H), 2.53-2.74 (200 MHz, CDCl₃) (m, 4H), 2.83-2.93 (m, 2H), 3.14 (d, J = 15.2 Hz, 1H), 3.23 (d, J = 15.2 Hz, 1H), 3.71 (s, 3H), 3.85 (s, 3H), 3.86 (s, 3H), 5.33 (s, 1H), 6.54-6.60 (m, 2H), 6.61 (s, 1H), 7.00-7.06 (m, 1H), 7.10-7.20 (m, 3H), 7.21-7.31 (m, 2H) ¹³C NMR δ 28.7, 29.2, 33.7, 50.5, 54.2, 55.4, 55.7, 56.0, 57.5, (50 MHz, CDCl₃) 99.1, 104.7, 110.3, 116.3, 122.5, 125.3, 127.0, 128.2, 129.3, 132.0, 138.6, 141.4, 145.2, 158.1, 160.8 EIHR-MS calcd for C₂₇H₃₂NO₄ [M + H]⁺, 434.2331; found, 434.2356 Compound number 141 Name 6-Methoxy-8-(2-methoxyphenyl)-2-(3-(4-nitro- phenyl)propyl)-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 1.69-1.90 (m, 2H), 2.29-2.45 (m, 2H), 2.60-2.78 (200 MHz, CDCl₃) (m, 4H), 2.83-2.96 (m. 2H), 3.11 (d, J = 15.2 Hz, 1H), 3.19 (d, J = 15.2 Hz, 1H), 3.75 (s, 3H), 3.88 (s, 3H), 5.37 (bs, 1H), 6.64 (s, 1H), 6.96-7.09 (m, 2H), 7.14 (dd, J = 7.3, 1.9 Hz, 1H), 7.22-7.32 (m, 2H), 7.32-7.43 (m, 1H), 8.05-8.16 (m, 2H) ¹³C NMR δ 28.4, 29.4, 33.5, 50.6, 54.2, 55.8, 56.0, 57.0, (50 MHz, CDCl₃) 110.3, 111.4, 121.0, 122.7, 123.7, 124.2, 125.2, 126.2, 129.3, 131.6, 141.2, 145.2, 146.4, 150.4, 157.1 ESI-MS m/z 449 ([M + H]⁺) EIHR-MS calcd for C₂₆H₂₉N₂O₅ [M + H]⁺, 449.2076; found, 449.2087 Compound number 142 Name 6-Methoxy-8-(2-methoxyphenyl)-2-(3-(2-nitro- phenyl)propyl)-1,2,3,4-tetrahydroisoquinolin-7-ol ¹H NMR δ 1.69-1.90 (m, 2H), 2.34-2.51 (m, 2H), 2.60-2.78 (200 MHz, CDCl₃) (m, 2H), 2.78-2.99 (m. 4H), 3.13 (d, J = 15.2 Hz, 1H), 3.23 (d, J = 15.2 Hz, 1H), 3.76 (s, 3H), 3.88 (s, 3H), 6.64 (s, 1H), 6.96-7.10 (m, 2H), 7.15 (dd, J = 7.3, 1.9 Hz, 1H), 7.24-7.29 (m, 1H), 7.32-7.40 (m, 1H), 7.61-7.76 (m, 2H), 7.82-7.92 (m, 1H) ¹³C NMR δ 28.1, 29.3, 30.8, 50.2, 54.3, 55.7, 56.0, 57.3, (50 MHz, CDCl₃) 110.3, 111.4, 120.9, 122.8, 124.1, 124.7, 125.4, 126.3, 127.0, 129.4, 131.6, 132.1, 132.9, 137.4, 141.1, 145.2, 149.4, 157.1 ESI-MS m/z 449 ([M + H]⁺) EIHR-MS calcd for C₂₆H₂₉N₂O₅ [M + H]⁺, 449.2076; found, 449.2098 Compound number 150 Name 8-Bromo-6,7-dimethoxy-2-phenethyl-1,2,3,4- tetrahydroisoquinoline ¹H NMR δ 2.71-2.94 (m, 8H), 3.63 (s, 2H), 3.82 (s, 3H), 3.83 (200 MHz, CDCl₃) (s, 3H), 6.63 (s, 1H), 7.20-7.31 (m, 5H) ¹³C NMR δ 29.7, 34.1, 50.2, 56.1, 56.4, 60.2, 60.6, 111.7, (50 MHz, CDCl₃) 118.2, 126.2, 126.8, 128.5, 128.8, 131.9, 140.4, 144.6, 151.7 ESI-MS m/z 376 ([M + H]⁺), 398 ([M + Na]⁺) EIHR-MS calcd for C₁₉H₂₃BrNO₂ [M + H]⁺, 376.0912; found, 376.0905 Compound number 152 Name 8-Bromo-6,7-dimethoxy-2-(4-nitrophenethyl)- 1,2,3,4-tetrahydroisoquinoline ¹H NMR δ 2.69-2.80 (m, 2H), 2.80-2.93 (m, 4H), 2.96-3.10 (200 MHz, CDCl₃) (m, 2H), 3.61 (s, 2H), 3.82 (s, 3H), 3.84 (s, 3H), 6.64 (s, 1H), 7.36-7.46 (m, 2H), 8.10-8.19 (m, 2H) ¹³C NMR δ 29.6, 33.9, 50.2, 56.2, 56.3, 59.1, 60.6, 111.7, (50 MHz, CDCl₃) 118.2, 123.8, 126.5, 129.7, 131.8, 144.7, 146.6, 148.4, 151.8 ESI-MS m/z 421 ([M + H]⁺), 443 ([M + Na]⁺) EIHR-MS calcd for C₁₉H₂₂BrN₂O₄ [M + H]⁺, 421.0763; found, 421.0730 Compound number 153 Name 8-Bromo-2-(2-chlorophenethyl)-6,7-dimethoxy- 1,2,3,4-tetrahydroisoquinoline ¹H NMR δ 2.73-2.95 (m, 6H), 2.99-3.13 (m, 2H), 3.66 (s, (200 MHz, CDCl₃) 2H), 3.82 (s, 3H), 3.84 (s, 3H), 6.64 (s, 1H), 7.10- 7.25 (m, 2H), 7.29-7.39 (m, 2H) ¹³C NMR δ 29.7, 31.7, 50.0, 56.2, 56.4, 58.0, 60.6, 111.8, (50 MHz, CDCl₃) 118.3, 126.9, 127.0, 127.8, 129.6, 131.0, 131.9, 134.2, 138.0, 144.6, 151.7 ESI-MS m/z 410 ([M + H]⁺) EIHR-MS calcd for C₁₉H₂₂BrClNO₂ [M + H]⁺, 410.0522; found, 410.0494 Compound number 154 Name 8-Bromo-2-(2-fluorophenethyl)-6,7-dimethoxy- 1,2,3,4-tetrahydroisoquinoline ¹H NMR δ 2.69-2.90 (m. 6H), 2.90-3.04 (m, 2H), 3.63 (s, (200 MHz, CDCl₃) 2H), 3.82 (s, 3H), 3.84 (s, 3H), 6.63 (s, 1H), 6.95- 7.12 (m, 2H), 7.12-7.33 (m, 2H) ¹³C NMR δ 27.3, 29.7, 50.0, 56.2, 56.4, 58.4, 60.6, 111.7, (50 MHz, CDCl₃) 115.3 (J = 22.0 Hz), 118.2, 124.2, 126.8, 127.1 (J = 16.1 Hz), 127.9 (J = 8.0 Hz), 131.1 (J = 4.8 Hz), 131.9, 144.6, 151.6, 161.3 (J = 243 Hz) ESI-MS m/z 394 ([M + H]⁺) EIHR-MS calcd for C₁₉H₂₂BrFNO₂ [M + H]⁺, 394.0818; found, 394.0806 Compound number 157 Name 8-(2-Fluorophenyl)-6,7-dimethoxy-2-phenethyl- 1,2,3,4-tetrahydroisoquinoline ¹H NMR δ 2.54-2.88 (m, 6H), 2.88-3.05 (m, 2H), 3.19 (d, J = (200 MHz, CDCl₃) 15.0 Hz, 1H), 3.30 (d, J = 15.0 Hz, 1H), 3.56 (s, 3H), 3.86 (s, 3H), 6.73 (s, 1H), 7.03-7.41 (m, 9H) ¹³C NMR δ 29.5, 34.0, 50.3, 54.2, 55.9, 60.0, 60.8, 112.5, (50 MHz, CDCl₃) 115.6 (J = 22.2 Hz), 123.6, 124.0 (J = 3.2 Hz), 126.1, 128.1, 128.4, 128.7, 129.4, 130.1, 131.8 (J = 3.5 Hz), 140.4, 145.2, 151.0, 159.9 (J = 234 Hz) ESI-MS m/z 392 ([M + H]⁺) EIHR-MS calcd for C₂₅H₂₇FNO₂ [M + H]⁺, 390.2026; found, 390.2014 Compound number 158 Name 8-(2-Chlorophenyl)-6,7-dimethoxy-2-phenethyl- 1,2,3,4-tetrahydroisoquinoline ¹H NMR δ 2.55-2.68 (m, 2H), 2.68-2.89 (m. 4H), 2.89-3.00 (200 MHz, CDCl₃) (m, 2H), 3.17 (s, 2H), 3.58 (s, 3H), 3.87 (s, 3H), 6.73 (s, 1H), 7.10-7.27 (m, 6H), 7.27-7.36 (m, 2H), 7.43-7.53 (m, 1H) ¹³C NMR δ 29.5, 34.0, 50.4, 53.9, 55.9, 60.0, 60.7, 112.3, (50 MHz, CDCl₃) 125.7, 126.1, 126.8, 128.4, 128.8, 129.0, 129.5, 130.1, 131.3, 131.8, 133.8, 135.6, 140.4, 144.6, 151.0 ESI-MS m/z 408 ([M + H]⁺) EIHR-MS calcd for C₂₅H₂₇ClNO₂ [M + H]⁺, 408.1730; found, 408.1730 Compound number 159 Name 6,7-Dimethoxy-8-(2-methoxyphenyl)-2-phenethyl- 1,2,3,4-tetrahydroisoquinoline ¹H NMR δ 2.54-2.87 (m, 6H), 2.87-3.00 (m. 2H), 3.15 (d, J = (200 MHz, CDCl₃) 15.1 Hz, 1H), 3.26 (d, J = 15.1 Hz, 1H), 3.52 (s, 3H), 3.74 (s, 3H), 3.86 (s, 3H), 6.69 (s, 1H), 6.92- 7.05 (m, 2H), 7.06-7.15 (m, 2H), 7.15-7.29 (m, 4H), 7.29-7.40 (m, 1H) ¹³C NMR δ 29.6, 34.0, 50.4, 54.1, 55.5, 55.8, 60.1, 60.6, (50 MHz, CDCl₃) 110.8, 111.8, 120.6, 125.2, 126.1, 126.3, 128.4, 128.8, 128.9, 129.6, 131.2, 140.5, 145.0, 151.0, 156.9 ESI-MS m/z 404 ([M + H]⁺) EIHR-MS calcd for C₂₆H₃₀NO₃ [M + H]⁺, 404.2226; found, 404.2217 Compound number 165 Name 2-(2-Fluorophenethyl)-8-(2-fluorophenyl)-6,7- dimethoxy-1,2,3,4-tetrahydroisoquinoline ¹H NMR δ 2.56-2.68 (m, 2H), 2.68-2.88 (m, 4H), 2.88-3.01 (200 MHz, CDCl₃) (m. 2H), 3.20 (d, J = 15.1 Hz, 1H), 3.31 (d, J = 15.1 Hz, 1H), 3.56 (s, 3H), 3.86 (s, 3H), 6.73 (s, 1H), 6.89-7.06 (m, 2H), 7.09-7.24 (m, 5H), 7.28-7.42 (m, 1H) ¹³C NMR δ 27.2, 29.5, 50.1, 54.2, 55.9, 58.2, 60.8, 112.6,, (50 MHz, CDCl₃) 115.3 (J = 21.7 Hz), 115.6 (J = 22.0 Hz), 123.6, 124.0 (J = 3.2 Hz), 126.1, 127.2 (J = 15.9 Hz), 127.8 (J = 7.9 Hz), 128.1, 129.5 (J = 7.9 Hz), 130.2, 131.0 (J = 4.9 Hz), 131.8 (J = 3.0 Hz), 145.2, 151.1, 159.9 (J = 244 Hz), 161.2 (J = 243 Hz) ESI-MS m/z 410 ([M + H]⁺) EIHR-MS calcd for C₂₅H₂₆F₂NO₂ [M + H]⁺, 410.1932; found, 410.1927 Compound number 166 Name 8-(2-Chlorophenyl)-2-(2-fluorophenethyl)-6,7- dimethoxy-1,2,3,4-tetrahydroisoquinoline ¹H NMR δ 2.55-2.68 (m, 2H), 2.68-2.88 (m, 4H), 2.88-3.00 (200 MHz, CDCl₃) (m. 2H), 3.18 (s, 2H), 3.57 (s, 3H), 3.87 (s, 3H), 6.73 (s, 1H), 6.88-7.05 (m, 2H), 7.06-7.24 (m, 3H), 7.26-7.36 (m, 2H), 7.42-7.52 (m, 1H) ¹³C NMR δ 27.2, 29.4, 50.1, 53.9, 55.9, 58.1, 60.7, 112.4, (50 MHz, CDCl₃) 115.3 (J = 22.0 Hz), 124.0 (J = 3.2 Hz), 125.6, 126.8, 127.2 (J = 16.0 Hz), 127.8 (J = 7.9 Hz), 129.0, 129.5, 130.1, 131.0 (J = 4.9 Hz), 131.3, 131.8, 133.8, 135.6, 144.7, 151.0, 161.2 (J = 243 Hz) ESI-MS m/z 426 ([M + H]⁺) EIHR-MS calcd for C₂₅H₂₆ClFNO₂ [M + H]⁺, 426.1636; found, 426.1634 Compound number 167 Name 2-(2-Chlorophenethyl)-8-(2-fluorophenyl)-6,7- dimethoxy-1,2,3,4-tetrahydroisoquinoline ¹H NMR δ 2.55-2.70 (m, 2H), 2.70-3.02 (m, 6H), 3.22 (d, J = (200 MHz, CDCl₃) 15.1 Hz, 1H), 3.32 (d, J = 15.1 Hz, 1H), 3.56 (s, 3H), 3.87 (s, 3H), 6.73 (s, 1H), 7.04-7.24 (m, 6H), 7.24-7.42 (m, 2H) ¹³C NMR δ 29.5, 31.5, 50.1, 54.3, 55.9, 57.9, 60.8, 112.5, (50 MHz, CDCl₃) 115.6 (J = 22.1 Hz), 123.6, 124.1, 126.1, 126.9, 127.6, 128.1, 129.4 (J = 7.1 Hz), 129.5, 130.1, 130.9, 131.9, 134.0, 137.9, 145.2, 151.1, 159.9 (J = 243 Hz) ESI-MS m/z 426 ([M + H]⁺) EIHR-MS calcd for C₂₅H₂₆ClFNO₂ [M + H]⁺, 426.1636; found, 426.1640 Compound number 168 Name 2-(2-Chlorophenethyl)-8-(2-chlorophenyl)-6,7- dimethoxy-1,2,3,4-tetrahydroisoquinoline ¹H NMR δ 2.53-2.69 (m, 2H), 2.69-3.03 (m, 6H), 3.20 (s, (200 MHz, CDCl₃) 2H), 3.57 (s, 3H), 3.87 (s, 3H), 6.73 (s, 1H), 7.02- 7.23 (m, 4H), 7.23-7.38 (m, 3H), 7.42-7.54 (m, 1H) ¹³C NMR δ 29.5, 31.6, 50.2, 54.0, 55.9, 57.9, 60.7, 112.4, (50 MHz, CDCl₃) 125.7, 126.8, 127.6, 129.0, 129.5, 130.1, 130.9, 131.3, 131.8, 133.8, 134.1, 135.7, 138.0, 144.7, 151.0 ESI-MS m/z 442 ([M + H]⁺) EIHR-MS calcd for C₂₅H₂₆Cl₂NO₂ [M + H]⁺, 442.1341; found, 442.1335 Compound number 171 Name 8-(2-Fluorophenyl)-6,7-dimethoxy-2-(4- nitrophenethyl)-1,2,3,4-tetrahydroisoquinoline ¹H NMR δ 2.62-3.00 (m, 8H), 3.20 (dd, J = 17.9, 15.1 Hz, (200 MHz, CDCl₃) 2H), 3.55 (s, 3H), 3.87 (s, 3H), 6.73 (s, 1H), 7.07- 7.24 (m, 3H), 7.25-7.42 (m, 3H), 8.04-8.15 (m, 2H) ¹³C NMR δ 29.6, 34.1, 50.5, 54.2, 55.9, 59.0, 60.8, 112.5, (50 MHz, CDCl₃) 115.7 (J = 22.3 Hz), 123.5, 123.7 (J = 17.4 Hz), 124.0, 125.8, 128.1, 129.5 (J = 7.3 Hz), 129.6, 130.0, 131.8 (J = 3.1 Hz), 145.3, 151.0, 161.2 (J = 243 Hz ESI-MS m/z 437 ([M + H]⁺) EIHR-MS calcd for C₂₅H₂₆FN₂O₄ [M + H]⁺, 437.1877; found, 437.1874 Compound number 172 Name 8-(2-Chlorophenyl)-6,7-dimethoxy-2-(4- nitrophenethyl)-1,2,3,4-tetrahydroisoquinolinee ¹H NMR δ 2.61-2.99 (m, 8H), 3.13 (dd, J = 16.6, 15.2 Hz, (200 MHz, CDCl₃) 2H), 3.57 (s, 3H), 3.87 (s, 3H), 6.73 (s, 1H), 7.11- 7.22 (m, 2H), 7.24-7.37 (m, 4H), 7.47-7.52 (m, 1H), 8.03-8.14 (m, 2H) ¹³C NMR δ 29.5, 34.0, 50.6, 53.9, 58.9, 60.7, 112.3, 123.7, (50 MHz, CDCl₃) 125.3, 126.9, 129.0. 129.6, 130.0, 131.3, 131.8, 133.7, 135.6, 144.7, 146.5, 148.6, 151.1 ESI-MS m/z 453 ([M + H]⁺) EIHR-MS calcd for C₂₅H₂₆ClN₂O₄ [M + H]⁺, 453.1581; found, 453.1571 Compound number 173 Name 6,7-Dimethoxy-8-(2-methoxyphenyl)-2-(4- nitrophenethyl)-1,2,3,4-tetrahydroisoquinoline ¹H NMR δ 2.59-3.00 (m, 8H), 3.17 (dd, J = 19.8, 15.0 Hz, (200 MHz, CDCl₃) 2H), 3.52 (s, 3H), 3.73 (s, 3H), 3.86 (s, 3H), 6.69 (s, 1H), 6.92-7.04 (m, 2H), 7.07 (dd, J = 7.4, 2.2 Hz, 1H), 7.26-7.41 (m, 3H), 8.03-8.14 (m, 2H) ¹³C NMR δ 29.6, 34.0, 50.6, 54.1, 55.5, 55.9, 59.0, 60.6, (50 MHz, CDCl₃) 110.8, 111.8, 120.6, 123.6, 125.1, 126.0, 129.0, 129.6, 131.1, 145.1, 146.5, 148.7, 151.1, 156.9 ESI-MS m/z 449 ([M + H]⁺) EIHR-MS calcd for C₂₆H₂₉N₂O₅ [M + H]⁺, 449.2076; found, 449.2071

The 5-HT_(2A) Receptor Binding Affinity of Compounds 116, 157 and 167.

The 5-HT_(2A) receptor binding affinity data are represented by K_(i) values. As shown in Table 8, the 5-HT_(2A) receptor binding affinity of compounds 116, 157 and 167 are higher than those of the well-known 5-HT_(2A) receptor antagonists, sarpogrelate and ketanserin.

TABLE 8 The 5-HT_(2A) receptor binding affinity data The present invention Prior-art (compound number) sarpogrelate ketanserin 116 157 167 K_(i) (nM) 8.39 3.5 3.47 2.21 0.119

Protective Effects of Post-Treatment of Multiple Doses of Compound 116 on LPS Induced Endotoxaemia in Mice Model:

12 hours after intraperitoneal injection of lipopolysaccharide (LPS) 100 mg/kg, compound 116 100 μg/kg or 300 μg/kg were administrated intraperitoneally or subcutaneously every 6 hour till 48 hours after LPS insults. FIG. 7 shows the result. Both 100 μg/kg and 300 μg/kg treatment of compound 116 shifted the survive curve rightward significantly compared to the vehicle control group (p<0.01.). Survival curves were compared by the Log rank test, and 3 days survival rate was compared by the chi square test.

Protective Effects of Post-Treatment of Multiple Doses of Compound 167 on LPS Induced Endotoxaemia in Mice Model:

The experiment method is the same as described above and FIG. 8 shows the result.

Compound 116 Did not Exert Platelet Activation, but Inhibited 5-HT Induced Amplification of Platelet Aggregation:

Blood samples were collected from male adult Spraque-Dawley rats, and platelet rich plasma (PRP) and platelet poor plasma (PPP) were obtained by centrifugation. Aggregation was elicited by adding collagen 3 μg/mL in PRP, and the aggregation response was recorded as the change of light transmission of PRP with Lumi-aggregometer. In FIG. 9 a, collagen induced platelet aggregation, and the aggregation response was amplified by adding 10 μM serotonin in 30 seconds before adding collagen, as shown in FIG. 9 b. The amplifying effects of serotonin was blocked by adding 10 μM ketanserin or 3 μg/mL compound 116 in 30 seconds before adding serotonin, as shown in FIG. 9 c and FIG. 9 d.

Compound 116 Inhibits Serotonin Induced Rat De-Endothelial Thoracic Descending Aorta Contraction:

Thoracic aortae were obtained from adult male Sprague Dawley rats. The aortae were cleared of adhering periadventitial fat and cut into strips 3-4 mm in length. Later, the relaxation in response to acetylcholine (1 μM) following PE (0.1 μM) was considered as evidence that the endothelium was intact. The tissue was incubated with warmed (37° C.), oxygenated (95% O₂/5% CO₂) Krebs-Henseleit solution (KBS, pH7.4) consisting of NaCl 118.2 mM, KCl 4.7 mM, KH₂PO₄ 1.2 mM, MgSO₄ 1.2 mM, CaCl₂·2H₂O 1.9 mM, NaHCO₃ 25 mM and glucose 11.7 mM. Indomethacin (10 μM) was added to prevent the production of prostanoids. One end of the segment was fixed to the organ bath chamber, and the other to a force transducer (Type BG 25; Gould, Oxnard, Calif., USA) in which tension is recorded (model RS 3400 recorder, Gould). The preparations were allowed to equilibrate for at least 60 min under a passive tension of 1.5±0.2 g. Cumulative responses to serotonin (30 nM-0.1 mM) were examined for 20 min after addition of 0.03 or 0.1 μM compound 116 to the organ bath. Contraction responses were expressed as the percentage of maximum contraction. As shown in FIG. 10, compound 116 inhibits serotonin induced smooth muscle contraction in a dose dependent manner.

EMBODIMENTS

-   1. A compound, comprising a formula of:

-   2. A compound as claimed in claim 1, providing an antagonism to a     5-HT_(2A) receptor. -   3. A compound as claimed in claim 1, inhibiting an aorta     contraction. -   4. A compound as claimed in claim 3, wherein the aorta contraction     is induced by a serotonin -   5. A compound as claimed in claim 1, inhibiting a platelet     aggregation. -   6. A compound as claimed in claim 5, wherein the platelet     aggregation is induced by a serotonin. -   7. A compound or a pharmaceutically acceptable salt thereof,     comprising a formula of:

-   -   wherein R₁ is one selected from a group consisting of C₃₋₁₂         linear chain alkyl group, C₁₋₁₂ branched chain alkyl group,         (CH₂)_(n)(Hete)R₁₀R₁₁R₁₂ and (CH₂)_(n)ArR₁₀R₁₁R₁₂, wherein the n         is an integer from 2 to 6, Hete is a heterocyclic group, and         R₁₀, R₁₁ and R₁₂ are independently selected from a group         consisting of hydrogen, halo group, nitro group, amino group,         cyano group, acetyl group, C₁₋₆ linear chain saturated alkyl         group, C₁₋₆ linear chain saturated alkoxy group and C₁₋₆ linear         chain saturated haloalkyl group;     -   Ar is an aryl group;     -   R₂ is one of a hydrogen and a C₁₋₆ linear chain saturated alkyl         group;     -   R₃ is one of a hydroxyl group and a C₁₋₆ linear chain saturated         alkoxy group;     -   R₄ is one of a hydroxyl group and a C₁₋₆ linear chain saturated         alkoxy group; and     -   X₁, X₂, X₃, X₄ and X₅ are independently selected from a group         consisting of hydrogen, halo group, nitro group, amino group,         cyano group, acetyl group, C₁₋₆ linear chain saturated alkyl         group, C₁₋₆ branched chain saturated alkyl group, C₁₋₆ linear         chain saturated alkoxy group, C₁₋₆ branched chain saturated         alkoxy group, C₁₋₆ linear chain saturated alkylthio group, C₁₋₆         branched chain saturated alkylthio group, C₁₋₆ linear chain         saturated haloalkyl group and C₁₋₆ branched chain saturated         haloalkyl group.

-   8. A compound as claimed in claim 7, wherein when any of R₁₀, R₁₁     and R₁₂ contains the halo group, the halo group is one selected from     a group consisting of fluorine, chlorine, bromine and iodine.

-   9. A compound as claimed in claim 7, wherein the heterocyclic group     is one selected from a group consisting of indolyl group, isoindolyl     group, indazolyl group, benzofuranyl group, isobenzofuranyl group,     benzothiophenyl group, benzimidazolyl group, benzoxazolyl group and     benzothiazolyl group, and the aryl group comprises a naphthyl group.

-   10. A pharmaceutical composition, comprising:     -   a pharmaceutically acceptable carrier; and     -   a therapeutically effective amount of a compound having a         formula of:

-   -   wherein R₁ is one selected from a group consisting of C₃₋₁₂         linear chain alkyl group, C₃₋₁₂ branched chain alkyl group,         (CH₂)_(n)(Hete)R₁₀R₁₁R₁₂ and (CH₂)_(n)ArR₁₀R₁₁R₁₂, wherein the n         is an integer from 2 to 6, Hete is a heterocyclic group, the Ar         is an aryl group, and R₁₀, R₁₁ and R₁₂ are independently         selected from a group consisting of hydrogen, halo group, nitro         group, amino group, cyano group, acetyl group, C₁₋₆ linear chain         saturated alkyl group, C₁₋₆ linear chain saturated alkoxy group         and C₁₋₆ linear chain saturated haloalkyl group;     -   R₂ is one of a hydrogen and a C₁₋₆ linear chain saturated alkyl         group;     -   R₃ is one of a hydroxyl group and a C₁₋₆ linear chain saturated         alkoxy group;     -   R₄ is one of a hydroxyl group and a C₁₋₆ linear chain saturated         alkoxy group; and     -   X₁, X₂, X₃, X₄ and X₅ are independently selected from a group         consisting of hydrogen, halo group, nitro group, amino group,         cyano group, acetyl group, C₁₋₆ linear chain saturated alkyl         group, C₁₋₆ branched chain saturated alkyl group, C₁₋₆ linear         chain saturated alkoxy group, C₁₋₆ branched chain saturated         alkoxy group, C₁₋₆ linear chain saturated alkylthio group, C₁₋₆         branched chain saturated alkylthio group, C₁₋₆ linear chain         saturated haloalkyl group and C₁₋₆ branched chain saturated         haloalkyl group.

-   11. A pharmaceutical composition as claimed in claim 10, wherein     when any of R₁₀, R₁₁ and R₁₂ contains the halo group, the halo group     is one selected from a group consisting of fluorine, chlorine,     bromine and iodine.

-   12. A pharmaceutical composition as claimed in claim 10, wherein the     heterocyclic group is one selected from a group consisting of     indolyl group, isoindolyl group, indazolyl group, benzofuranyl     group, isobenzofuranyl group, benzothiophenyl group, benzimidazolyl     group, benzoxazolyl group and benzothiazolyl group and the aryl     group comprises naphthyl group.

-   13. A method of treating a sepsis, comprising a step of     administering to a subject in need thereof an effective amount of     the pharmaceutical composition of claim 10. 

What is claimed is:
 1. A compound, comprising a formula of:


2. A compound as claimed in claim 1, providing an antagonism to a 5-HT2A receptor.
 3. A compound as claimed in claim 1, inhibiting an aorta contraction.
 4. A compound as claimed in claim 3, wherein the aorta contraction is induced by a serotonin.
 5. A compound as claimed in claim 1, inhibiting a platelet aggregation.
 6. A compound as claimed in claim 5, wherein the platelet aggregation is induced by a serotonin.
 7. A compound or a pharmaceutically acceptable salt thereof, comprising a formula of:

wherein R₁ is one selected from a group consisting of C₃₋₁₂ linear chain alkyl group, C₃₋₁₂ branched chain alkyl group, (CH₂)_(n)(Hete)R₁₀R₁₁R₁₂ and (CH₂)_(n)ArR₁₀R₁₁R₁₂, wherein the n is an integer from 2 to 6, Hete is a heterocyclic group, and R₁₀, R₁₁ and R₁₂ are independently selected from a group consisting of hydrogen, halo group, nitro group, amino group, cyano group, acetyl group, C₁₋₆ linear chain saturated alkyl group, C₁₋₆ linear chain saturated alkoxy group and C₁₋₆ linear chain saturated haloalkyl group; Ar is an aryl group; R₂ is one of a hydrogen and a C₁₋₆ linear chain saturated alkyl group; R₃ is one of a hydroxyl group and a C₁₋₆ linear chain saturated alkoxy group; R₄ is one of a hydroxyl group and a C₁₋₆ linear chain saturated alkoxy group; and X₁, X₂, X₃, X₄ and X₅ are independently selected from a group consisting of hydrogen, halo group, nitro group, amino group, cyano group, acetyl group, C₁₋₆ linear chain saturated alkyl group, C₁₋₆, branched chain saturated alkyl group, C₁₋₆ linear chain saturated alkoxy group, C₁₋₆ branched chain saturated alkoxy group, C₁₋₆ linear chain saturated alkylthio group, C₁₋₆ branched chain saturated alkylthio group, C₁₋₆ linear chain saturated haloalkyl group and C₁₋₆ branched chain saturated haloalkyl group.
 8. A compound as claimed in claim 7, wherein when any of R₁₀, R₁₁ and R₁₂ contains the halo group, the halo group is one selected from a group consisting of fluorine, chlorine, bromine and iodine.
 9. A compound as claimed in claim 7, wherein the heterocyclic group is one selected from a group consisting of indolyl group, isoindolyl group, indazolyl group, benzofuranyl group, isobenzofuranyl group, benzothiophenyl group, benzimidazolyl group, benzoxazolyl group and benzothiazolyl group, and the Ar is an aryl group comprising a naphthyl group.
 10. A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier; and a therapeutically effective amount of a compound having a formula of:

wherein R₁ is one selected from a group consisting of C₃₋₁₂ linear chain alkyl group, C₃₋₁₂ branched chain alkyl group, (CH₂)_(n)(Hete)R₁₀R₁₁R₁₂ and (CH₂)_(n)ArR₁₀R₁₁R₁₂, wherein the n is an integer from 2 to 6, Hete is a heterocyclic group, and R₁₀, R₁₁ and R₁₂ are independently selected from a group consisting of hydrogen, halo group, nitro group, amino group, cyano group, acetyl group, C₁₋₆ linear chain saturated alkyl group, C₁₋₆ linear chain saturated alkoxy group and C₁₋₆ linear chain saturated haloalkyl group; Ar is an aryl group; R₂ is one of a hydrogen and a C₁₋₆ linear chain saturated alkyl group; R₃ is one of a hydroxyl group and a C₁₋₆ linear chain saturated alkoxy group; R₄ is one of a hydroxyl group and a C₁₋₆ linear chain saturated alkoxy group; and X₁, X₂, X₃, X₄ and X₅ are independently selected from a group consisting of hydrogen, halo group, nitro group, amino group, cyano group, acetyl group, C₁₋₆ linear chain saturated alkyl group, C₁₋₆ branched chain saturated alkyl group, C₁₋₆ linear chain saturated alkoxy group, C₁₋₆ branched chain saturated alkoxy group, C₁₋₆ linear chain saturated alkylthio group, C₁₋₆ branched chain saturated alkylthio group, C₁₋₆ linear chain saturated haloalkyl group and C₁₋₆ branched chain saturated haloalkyl group.
 11. A pharmaceutical composition as claimed in claim 10, wherein when any of R₁₀, R₁₁ and R₁₂ contains the halo group, the halo group is one selected from a group consisting of fluorine, chlorine, bromine and iodine.
 12. A pharmaceutical composition as claimed in claim 10, wherein the heterocyclic group is one selected from a group consisting of indolyl group, isoindolyl group, indazolyl group, benzofuranyl group, isobenzofuranyl group, benzothiophenyl group, benzimidazolyl group, benzoxazolyl group and benzothiazolyl group and the Ar is aryl group comprising naphthyl group.
 13. A method of treating a sepsis, comprising a step of administering to a subject in need thereof an effective amount of the pharmaceutical composition of claim
 10. 